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Carbon Dioxide → 8-Methylsulfonyl-12-hydroxy-5-heptadecynoic acid

HRID 263005
노트
인쇄 미리보기

반응식

HRID 263005 반응식
C[O:2][C:3]([CH2:5][CH2:6][CH2:7][C:8]#[C:9][CH2:10][C:11]([CH2:22][CH2:23][CH2:24][CH:25]([O:31]C(=O)C)[CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])([S:17](OC)(=[O:19])=[O:18])C(OCC)=O)=[O:4].[Cl-].[Na+].[C:37](=O)=O>CCOCC.O.CS(C)=O>[CH3:37][S:17]([CH:11]([CH2:22][CH2:23][CH2:24][CH:25]([OH:31])[CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH2:10][C:9]#[C:8][CH2:7][CH2:6][CH2:5][C:3]([OH:2])=[O:4])(=[O:19])=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 280Carbon DioxideHCID 5234Sodium ChlorideHCID 53799130HCID 53799130, 화합물

생성물 1

HCID 213176278-Methylsulfonyl-12-hydroxy-5-heptadecynoic acid

시약·촉매·용매 3

HCID 679Dimethyl Sulfoxide용매HCID 962Water용매2회
HCID 3283
Diethyl Ether
용매

실험 절차

A solution of ethyl 2-(6-methoxycarbonyl-2-hexyn-1-yl)-2-(4-acetoxynonyl)-2-(methoxysulfonyl)-acetate (48.8 g., 0.1 mole), water (3.6 g., 0.2 mole), and sodium chloride (6.5 g., 0.11 mole) in 120 ml. of dimethyl sulfoxide is heated at 130°-150° C. for 6 hours until evolution of carbon dioxide is completed. The mixture is cooled, treated with 400 ml. of water and the oily product taken up in ether, washed with water and dried over sodium sulfate. Evaporation of the ether in vacuo leaves the title compound as a yellow viscous oil.

후처리

  1. temperatureThe mixture is cooled
  2. additiontreated with 400 ml
  3. washwashed with water
  4. dry with materialdried over sodium sulfate
  5. customEvaporation of the ether in vacuo

출처 및 근거

ORD 기록
ord-d0e196a6f6984b4fa7746c2c07043a68
출처 데이터셋
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04155908

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