Nitric Acid → Ricinelaidic acid

HRID 426933

반응식

HRID 426933 반응식
[OH:1][C:2]([OH:23])(O)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19](O)=O.[N+]([O-])(O)=[O:25].N([O-])=O.[Na+]>O.C([O-])(=O)CCCCCCC/C=C\C[C@@H](CCCCCC)O.[Zn+2].C([O-])(=O)CCCCCCC/C=C\C[C@@H](CCCCCC)O>[C:2]([OH:23])(=[O:1])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9]/[CH:10]=[CH:11]/[CH2:12][C@@H:13]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[OH:25]

참가 물질

6

실험 절차

The castor oil acids from 50 kg of castor oil, obtained according to (1) and (2), are warmed in the crude state with 20 l of 50% strength HNO3 (50°-60°). A solution of 1.2 kg of sodium nitrite in 15 l of water is run in whilst stirring well, and the mixture is kept at 50°-60° C. for a further 10 minutes and then rapidly cooled, for example by pouring it onto ice. The reaction product separated from the aqueous phase can be further processed in the crude state like castor oil acid; the pure ricinelaidic acid is obtained by extracting the reaction product with boiling ligroin and crystallizing out by cooling.

후처리

  1. additionby pouring it onto ice
  2. customThe reaction product separated from the aqueous phase

출처 및 근거

ORD 기록
ord-3db2f1eb492349ef89adc88b6e65ea34
출처 데이터셋
uspto-grants-1979_10
특허 번호
US04172123

연결된 노트

불러오는 중…