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Triethylamine → N-methoxy-N-methyl-4-(pentafluoro-lambda6-sulfanyl)benzamide

HRID 1523310
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HRID 1523310 반응식
[F:1][S:2]([F:15])([F:14])([F:13])([F:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=[O:8])=[CH:5][CH:4]=1.Cl.[CH3:17][O:18][NH:19][CH3:20].C(N(CC)CC)C>ClCCl>[CH3:17][O:18][N:19]([CH3:20])[C:7](=[O:8])[C:6]1[CH:10]=[CH:11][C:3]([S:2]([F:15])([F:14])([F:13])([F:12])[F:1])=[CH:4][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 81138Methanamine, N-methoxy-, hydrochloride (1:1)HCID 27792154-(Pentafluorosulfanyl)benzoyl chloride

생성물 1

HCID 58360637N-methoxy-N-methyl-4-(pentafluoro-lambda6-sulfanyl)benzamide수율 51%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

4-(Pentafluoro-λ6-sulfanyl)benzoyl chloride (1.00 g, 3.751 mmol), O,N-dimethyl-hydroxylamine hydrochloride (0.402 g, 4.13 mmol), and triethylamine (0.835 g, 8.25 mmol) were stirred in dichloromethane for 2 hours at room temperature. The reaction was concentrated in vacuo and diethyl ether added. The solid was collected by filtration and purified by silica gel column chromatography to afford the title compound as a solid (0.557 g, 51% yield).

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후처리

  1. concentrationThe reaction was concentrated in vacuo and diethyl ether
  2. additionadded
  3. filtrationThe solid was collected by filtration
  4. custompurified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-50c7cfac7e1041dba3a139d5a554d541
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09079878B2

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