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SU107266A1 - Phenyldichlorophosphine release method - Google Patents

Phenyldichlorophosphine release method

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Publication number
SU107266A1
SU107266A1 SU567281A SU567281A SU107266A1 SU 107266 A1 SU107266 A1 SU 107266A1 SU 567281 A SU567281 A SU 567281A SU 567281 A SU567281 A SU 567281A SU 107266 A1 SU107266 A1 SU 107266A1
Authority
SU
USSR - Soviet Union
Prior art keywords
phenyldichlorophosphine
reaction
release method
phosphorus
mixture
Prior art date
Application number
SU567281A
Other languages
Russian (ru)
Inventor
Е.Л. Гефтер
Original Assignee
Е.Л. Гефтер
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Е.Л. Гефтер filed Critical Е.Л. Гефтер
Priority to SU567281A priority Critical patent/SU107266A1/en
Application granted granted Critical
Publication of SU107266A1 publication Critical patent/SU107266A1/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Description

Фенилдихлорфосфин  вл етс  одним из важнейших фосфорорганических Гоединений.Phenyldichlorophosphine is one of the most important organophosphorus compounds.

В известном способе liO.IVieiJllFrIn a known way liO.IVieiJllFr

фе;1и; д11хлор(|х)С(|)ииа в;)аимодеГ1CiiiMCM бензо.ш li трехх.юристого фосфора 15 присутствии хлористого а, продукт выдел ют из рсакциоииой массы путем укстратиpOlKllii ; СТрОЛеЙ1И51Л1 Э{|)ИрОМ.fe; 1i; 11 Chloro (| x) C (|) IIa b;) isomodeH1CiiiMCM benzo.sh li trihuric phosphorus 15 in the presence of chloride a, the product is isolated from the x-ray mass by means ofOlKllii; STROLEY1I51L1 E {|) IROM.

П ред. i Hiiiii способ .леич1  феиилднхлорфосф|И1а из реакциониоП массы, иолучешгой изаимодейCTBiieM 6wf3o.ia и трехх.пористого фос{1)орг1 15 присутствии хлористого а.гюмпиии, состоит л том, что по ок(Л1чаи1И1 основиой реакции отгон ют избыток трсхх.юристого фосфора , к реакциоииой массе 1 рибавл ют ииридин дл  св зывани  х.торис1ого а.момиии  и фстпалдихдорфоссЬриг выдел ют перегонкой, 11 р и м с р. Пос.че проведе П1  основHoii реакц1 и взаимодействи  беизо .ла 39 ч., треххлористого фосфора 206 ч., в ирисутств - И х.тористого а.чюмиии  70 ч. путем кип чени  с обратным холодильником смеси в. течение 3-4 часов при энергичном неремеип1ванни реакционную массу охлаждают и отгон ют избыток т)ехх.тористо|-о фосфора при . 30-Ed. i Hiiiii method. leich1 feyildhlnosphosph | I1a from the reaction of the mass, and on the basics iz imodeyCTBiieM 6wf3o.ia and three-porous phos {1) org1 15 in the presence of a.ch. phosphorus, to the reaction mass 1 of the ribavl iiridine to bind the h of the secondary monomer and fstpaldihdorfosshrig are separated by distillation, 11 p and m s r. Poc. having a p1 base of the hiiii reaction and a beistole interaction 39 hours, phosphorus chloride 206 hours, in the iris - And ch.oristoy.chumyii 70 hours by boiling with a holo The mixture is mixed for 3-4 hours with energetic non-intermechanical reaction mixture is cooled and the excess t-exxoristo | -o phosphorus is distilled off at. thirty-

40.1ьи остаточного давлени  и температуре 50-55. К оставшейс  жндкостн добавл ют при неремешива1П и 42 ч. сухого пиридина, поддержива  температуру реакциоиггой смеси 40-50 По.лученную реакционную массу нагревают до 60- 70 н отгон ют в вакууме нлн токе СО; при перемсшивапии легко .летучую (|)ракц1ПО, соде|5жаи1ую остатки трехх.лористого (|юсфора и пирил,ииа, а затем-техиичесьсий фени .тд.ихлор1|х)С(Ьии в кол1г-1еелве 83 ч. ( 93- от леории).40.1 residual pressure and temperature 50-55. To the remaining liquid is added with unmixing and 42 parts of dry pyridine, maintaining the temperature by reacting the mixture with 40-50 mixture. The reaction mixture is heated to 60–70 n and distilled in a vacuum of CO; in case of re-joining, easily volatile (|) rakts1PO, soda | 5zhai1uyu remains of trichloride (| yusfor and pyryl, ia, and then technical pheni. t.ichlor1 | x) S (Lii in kol1g-1eelva 83 h. (93- from Leoria).

При г1О1 тор11ой перегонке по.гучают 80 ч. чг1ст,)го с температурой кипепи  58-59 (0,8-At r1O1, the top distillation, 80 parts of ppm,) with a boiling point of 58-59 (0.8-

i .i.

Способ вьгделепн  фепп,лд1 хлорфос ()ииа из реакциоииой массы, полученной взаимодействием бензола и треххлор;тстого фосфора в присутствии х.юристого а;поми1Н1 , о т ,л и ч а ю HI; и и с   тем, что, с це.тыо упрои1еии  процесса и гговышепи  выхода, из реакционной масс1-л но OKOir-iain-nr основной реакци ) отгон ют избыток трехх.лориЛ1; 107266стого фосфора, св зывают хлориСТЫ11 алюминий прибавлением пи2 - ридипа и выдел ют nepeioiiKOH фенилднхлорфосфин .The method is limited to the reaction, ld1 chlorophos () and from the reaction mass obtained by the interaction of benzene and trichloro; solid phosphorus in the presence of h.yurist a; pom1N1, o t, l and h hI; and with the fact that, from the point of view of the management of the process and of the yield, the excess three-hloril1 is distilled off from the reaction mass (1 liter but OKOir-iain-nr main reaction); Phosphorus 107266 binds aluminum chlorides11 by adding pi2-ridip and nepeioiiKOH phenyl chlorophosphine is isolated.

SU567281A 1957-02-04 1957-02-04 Phenyldichlorophosphine release method SU107266A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU567281A SU107266A1 (en) 1957-02-04 1957-02-04 Phenyldichlorophosphine release method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU567281A SU107266A1 (en) 1957-02-04 1957-02-04 Phenyldichlorophosphine release method

Publications (1)

Publication Number Publication Date
SU107266A1 true SU107266A1 (en) 1957-11-30

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
SU567281A SU107266A1 (en) 1957-02-04 1957-02-04 Phenyldichlorophosphine release method

Country Status (1)

Country Link
SU (1) SU107266A1 (en)

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