SU107266A1 - Phenyldichlorophosphine release method - Google Patents
Phenyldichlorophosphine release methodInfo
- 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
Links
Landscapes
- 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.
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
ID=48380483
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) |
-
1957
- 1957-02-04 SU SU567281A patent/SU107266A1/en active
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