AT230881B - Process for the preparation of propionic acid-3,4-dichloroanilide - Google Patents
Process for the preparation of propionic acid-3,4-dichloroanilideInfo
- Publication number
- AT230881B AT230881B AT755662A AT755662A AT230881B AT 230881 B AT230881 B AT 230881B AT 755662 A AT755662 A AT 755662A AT 755662 A AT755662 A AT 755662A AT 230881 B AT230881 B AT 230881B
- Authority
- AT
- Austria
- Prior art keywords
- sep
- propionic acid
- dichloroanilide
- preparation
- chlorobenzene
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Herstellung von Propionsäure-3, 4-dichloranilid
EMI1.1
EMI1.2
<tb>
<tb>
4-dichlor-Analyse <SEP> : <SEP>
<tb> Gef. <SEP> : <SEP> C <SEP> : <SEP> 49, <SEP> 50% <SEP> H <SEP> : <SEP> 4, <SEP> 18% <SEP>
<tb> 49. <SEP> 59alto <SEP> 4, <SEP> 21%
<tb> Ber. <SEP> : <SEP> C <SEP> : <SEP> 49, <SEP> 55% <SEP> H <SEP> : <SEP> 4, <SEP> 13% <SEP>
<tb>
<Desc/Clms Page number 2>
b) Die Aufarbeitung der Chlorbenzollösung kann auch so'erfolgen : Im Wasserstrahlvakuum werden41 Chlorbenzol mit dem restlichen Propionsäurechlorid abdestilliert, dann wird die hinterbleibende Lösung auf 5-10 C abgekühlt und einige Stunden auf dieser Temperatur gehalten. Beim Filtrieren werden 47% d. Th. des Propionsäure-3, 4-dichloranilids vom F : 87 - 9l0C erhalten.
Wird die Mutterlauge aus dieser Reaktion in einem nächsten Versuch wieder eingesetzt, so steigt in diesem Ansatz die Ausbeute weiter an und das Produkt schmilzt bei 89-92 C.
PATENTANSPRÜCHE :
1. Verfahren zur Herstellung von Propionsäure-3, 4-dichloranilid, dadurch gekennzeichnet, dass Propionsäure und 3, 4-Dichloranilin in Chlorbenzol in Gegenwart eines Überschusses Thionylchlorid umgesetzt werden.
<Desc / Clms Page number 1>
Process for the preparation of propionic acid-3,4-dichloroanilide
EMI1.1
EMI1.2
<tb>
<tb>
4-dichloro analysis <SEP>: <SEP>
<tb> Found <SEP>: <SEP> C <SEP>: <SEP> 49, <SEP> 50% <SEP> H <SEP>: <SEP> 4, <SEP> 18% <SEP>
<tb> 49. <SEP> 59alto <SEP> 4, <SEP> 21%
<tb> Ber. <SEP>: <SEP> C <SEP>: <SEP> 49, <SEP> 55% <SEP> H <SEP>: <SEP> 4, <SEP> 13% <SEP>
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<Desc / Clms Page number 2>
b) The chlorobenzene solution can also be worked up as follows: Chlorobenzene and the remaining propionic acid chloride are distilled off in a water jet vacuum, then the remaining solution is cooled to 5-10 ° C. and kept at this temperature for a few hours. When filtering, 47% d. Th. Of propionic acid-3, 4-dichloroanilide from F: 87-910C.
If the mother liquor from this reaction is used again in a next experiment, the yield increases further in this batch and the product melts at 89-92 ° C.
PATENT CLAIMS:
1. A process for the preparation of propionic acid-3,4-dichloroanilide, characterized in that propionic acid and 3,4-dichloroaniline are reacted in chlorobenzene in the presence of an excess of thionyl chloride.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE230881X | 1961-11-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT230881B true AT230881B (en) | 1963-12-30 |
Family
ID=5872760
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT755662A AT230881B (en) | 1961-11-10 | 1962-09-24 | Process for the preparation of propionic acid-3,4-dichloroanilide |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT230881B (en) |
-
1962
- 1962-09-24 AT AT755662A patent/AT230881B/en active
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