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Acetyl chloride → HCID 54159639, 화합물

HRID 1456339
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HRID 1456339 반응식
[C:1](Cl)(=[O:3])[CH3:2].[CH3:5][C:6]1[N:7]=[C:8]([C:12]([C:18]2[S:19][C:20]([CH3:24])=[C:21]([CH3:23])[N:22]=2)([OH:17])[C:13]([F:16])([F:15])[F:14])[S:9][C:10]=1[CH3:11]>CN(C)C1C=CN=CC=1.ClCCl>[C:1]([O:17][C:12]([C:8]1[S:9][C:10]([CH3:11])=[C:6]([CH3:5])[N:7]=1)([C:18]1[S:19][C:20]([CH3:24])=[C:21]([CH3:23])[N:22]=1)[C:13]([F:15])([F:16])[F:14])(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6367Acetyl chlorideHCID 22106686HCID 22106686, 화합물

생성물 1

HCID 54159639HCID 54159639, 화합물

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매HCID 6344Dichloromethane용매

실험 절차

Acetyl chloride (0.68 ml) was added to a solution of 1,1-bis (4,5-dimethyl-2-thiazolyl)-2,2,2-trifluoroethanol (1.54 g) and 4-dimethylaminopyridine (2 g) in dry dichloromethane (70 ml). The mixture was stirred at room temperature overnight and was then washed with saturated aqueous sodium hydrogen carbonate solution. The organic phase was separated, dried and evaporated and the residue was purified by flash chromatography to give the title compound. M.p. 163°-164° C. Found: C, 45.9; H, 4.0; N, 7.4. C14H15F3N2OS2 requires C, 46.15; H, 4.15; N, 7.7%

후처리

  1. washwas then washed with saturated aqueous sodium hydrogen carbonate solution
  2. customThe organic phase was separated
  3. customdried
  4. customevaporated
  5. customthe residue was purified by flash chromatography

출처 및 근거

ORD 기록
ord-f6b402b61cfe474ca56d34abeeff478e
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05843971

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