Pyridine → HCID 86762710, 화합물

HRID 74324노트

반응식

HRID 74324 반응식
[CH2:1](O)[CH2:2]/[CH:3]=[CH:4]\[CH2:5][CH2:6]/[CH:7]=[CH:8]\[CH:9]=[CH:10]\[CH2:11][CH3:12].N1C=CC=CC=1.CN(C)C=O.CS([Cl:29])(=O)=O>CCCCCC.O>[Cl:29][CH2:1][CH2:2]/[CH:3]=[CH:4]\[CH2:5][CH2:6]/[CH:7]=[CH:8]\[CH:9]=[CH:10]\[CH2:11][CH3:12]

참가 물질

7

반응 조건

온도
7.5 °C

실험 절차

(Z,Z,E)-3,7,9-Dodecatrien-1-ol (169.47 g, 0.94 mol), pyridine (134.2 g, 1.70 mol) and N,N-dimethylformamide (284 g) were placed in a reaction vessel, and stirred at 5 to 10° C. for 30 minutes. After stirring, methanesulfonyl chloride (151.2 g, 1.32 mol) was added dropwise thereto at 5 to 15° C. After completion of the dropwise addition, the reaction mixture was stirred at 60 to 65° C. for 2 hours. Then, water (471 g) was added to the reaction mixture to terminate the reaction. Hexane (471 g) was added thereto to separate the reaction mixture into phases. The organic phase was washed with hydrochloric acid and then with an aqueous sodium bicarbonate solution, and then concentrated by removal of the solvent under reduced pressure. The residue was distilled under reduced pressure to obtain (Z,Z,E)-1-chloro-3,7,9-dodecatriene (bp: 114 to 120° C./5 mmHg, 166.93 g, 0.84 mol) with a yield of 89.2%.

후처리

  1. stirringAfter stirring
  2. customat 5 to 15° C
  3. additionAfter completion of the dropwise addition
  4. stirringthe reaction mixture was stirred at 60 to 65° C. for 2 hours
  5. customto terminate
  6. customthe reaction
  7. customto separate the reaction mixture into phases
  8. washThe organic phase was washed with hydrochloric acid
  9. concentrationwith an aqueous sodium bicarbonate solution, and then concentrated by removal of the solvent under reduced pressure
  10. distillationThe residue was distilled under reduced pressure

출처 및 근거

ORD 기록
ord-35ca9c29b0764a1cadceb029af52b8c9
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08829255B1

반응 노트

불러오는 중…