CH254996A - Process for the production of reductic acid. - Google Patents
Process for the production of reductic acid.Info
- Publication number
- CH254996A CH254996A CH254996DA CH254996A CH 254996 A CH254996 A CH 254996A CH 254996D A CH254996D A CH 254996DA CH 254996 A CH254996 A CH 254996A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- reductic acid
- reductic
- acid
- hydrolysis
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/64—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of functional groups containing oxygen only in singly bound form
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung von Reduktinsäure. Das Hauptpatent betrifft ein Verfahren zur Herstellung von Reduktinsäure, welches dadurch gekennzeichnet ist, dass man 3-Ha- logen-cyklopenten-(2)-ol-(2)-on-(1) hydroly- #iert.
Es wurde dort vorgesehen, die Hydro- lyc= mit Hilfe eines schwach alkalischen Stoffes auszuführen.
Es wurde nun gefunden, dass man eine bührre Ausbeute bei einer genügend grossen 113-drolysegeschwindigkeit dadurch erhal- 1en kann, dass man das Ausgangsmaterial bei einer Temperatur über 100 C mit Wasser oder 'Wasserdampf erhitzt.
Beispiel <I>1:</I> In einem geschlossenen Gefäss wird 1 Ge- uicht#teil 3-Brom-ayklopenten- (2) -o1- (2)- on-(l) in,einer Stickstoffatmosphäre mit 15 (1r(-wicht teilen ausgekochten Wassers wäh rend einer Stunde auf 140"C erhitzt.
Aus einer Titration der gelbbraunen Flüssigkeit riiii: Jodlösung geht hervor, dass die Brom verbindung sich quantitativ in R.eduktinsäure umgewandelt hat. Man kann die Isolierung derselben z. B. dadurch vornehmen, dass man die warme Lösung mit Norit entfärbt (bei 200 C ausgedämpft) und im Vakuum zu einem kleinen Volumen einengt. HieTbei kristallisiert die Reduktinsäure aus.
<I>Beispiel 2:</I> In einem geschlossenen Gefäss wird 1 Ge- wichtisteil 3-Chlor-cyklo@penten-(2)-of-(2)-on- (1) in einer Stickstoffatmosphäre mit 15 Ge wichtsteilen ausgekochten Wassers während 11/2 Stunde auf 150-155 C (oder 3 Stunden auf 140 C) erhitzt. Die Farbe der Lösung ist etwas heller als bei der Hydrolyse der Bromverbindung. Die Ausbeute beträgt nach Titra,tion ungefähr 95 %. Die Isolierung kann wie in Beispiel 1 beschrieben stattfinden.
Process for the production of reductic acid. The main patent relates to a process for the production of reductic acid, which is characterized in that 3-halo-cyclopentene- (2) -ol- (2) -one- (1) is hydrolyzed.
It was planned there to carry out the Hydrolyc = with the help of a weakly alkaline substance.
It has now been found that a poor yield can be obtained at a sufficiently high rate of drolysis by heating the starting material with water or steam at a temperature above 100.degree.
Example <I> 1: </I> 1 portion of 3-bromo-ayklopenten- (2) -o1- (2) -on- (l) in a nitrogen atmosphere with 15 (1r (-weight parts of boiled water heated to 140 ° C for one hour.
A titration of the yellow-brown liquid riiii: iodine solution shows that the bromine compound has been converted quantitatively into reduced reductic acid. You can isolate the same z. B. can be done by decolorizing the warm solution with Norit (steamed out at 200 C) and concentrating in a vacuum to a small volume. The reductic acid crystallizes out.
<I> Example 2: </I> 1 part by weight of 3-chloro-cyklo @ penten- (2) -of- (2) -on- (1) is boiled in a nitrogen atmosphere with 15 parts by weight Water heated to 150-155 ° C. (or 3 hours at 140 ° C.) for 11/2 hours. The color of the solution is slightly lighter than when the bromine compound was hydrolyzed. The yield after titration is approximately 95%. The isolation can take place as described in Example 1.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL254996X | 1943-03-25 | ||
CH245669T | 1943-05-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH254996A true CH254996A (en) | 1948-05-31 |
Family
ID=25729068
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH254996D CH254996A (en) | 1943-03-25 | 1943-05-04 | Process for the production of reductic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH254996A (en) |
-
1943
- 1943-05-04 CH CH254996D patent/CH254996A/en unknown
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