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Isobutyl mercaptan → HCID 73207931, 화합물

HRID 2179916
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HRID 2179916 반응식
[CH3:1][CH:2]([CH3:5])[CH2:3][SH:4].[CH3:6][C@H:7]1[C:25](=[O:26])[O:24][C@H:9]2[CH2:10][C@:11]3([CH3:23])[O:13][C@H:12]3[C@@H:14]3[O:16][C@@H:15]3[C:17]3[C:21](=[O:22])[O:20][C@@H:19]([C@H:8]12)[CH:18]=3.CN(C1C=CC=CN=1)C>CC(C)=O>[OH:16][CH:14]1[CH:15]([S:4][CH2:3][CH:2]([CH3:5])[CH3:1])[C:17]2=[CH:18][CH:19]([O:20][C:21]2=[O:22])[CH:8]2[CH:9]([O:24][C:25](=[O:26])[CH:7]2[CH3:6])[CH2:10][C:11]2([CH3:23])[CH:12]1[O:13]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10558Isobutyl mercaptanHCID 218852-DimethylaminopyridineHCID 442200Dihydromikanolide

생성물 1

HCID 73207931HCID 73207931, 화합물수율 65.4%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

2-methyl-1-propanethiol (500 μmol; 54 μl) is added to a solution of dihydromikanolide (100 μmol; 30 mg) and dimethylaminopyridine (10 μmol; 1.2 mg) in acetone (1 ml). The reaction mass is stirred for two hours at ambient temperature then the solvent is evaporated off under reduced pressure. The residue is taken up in ether then the precipitate formed is filtered, washed with ether and dried under vacuum. 25 mg of product is obtained in the form of a white powder.

후처리

  1. customthe solvent is evaporated off under reduced pressure
  2. customthe precipitate formed
  3. filtrationis filtered
  4. washwashed with ether
  5. customdried under vacuum

출처 및 근거

ORD 기록
ord-9750054de80d443b9442c248867a3046
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06887869B2

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