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Methanesulfonyl chloride → HCID 90037025, 화합물

HRID 1055423
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HRID 1055423 반응식
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[F:6][CH:7]([F:21])[O:8][C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]=1[CH2:19][OH:20]>C(Cl)Cl>[CH3:1][S:2]([O:20][CH2:19][C:10]1[C:11]2[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:17]=[CH:18][C:9]=1[O:8][CH:7]([F:21])[F:6])(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 43394581[2-(Difluoromethoxy)naphthalen-1-yl]methanol

생성물 1

HCID 90037025HCID 90037025, 화합물수율 65.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Methanesulfonyl chloride (160 μL, 2.07 mmol) was added to a mixture of (2-(difluoromethoxy)naphthalen-1-yl)methanol (387 mg, 1.73 mmol) in CH2Cl2 (8.63 mL) and TEA (505 μL, 3.62 mmol). After 20 h the mixture was diluted with CH2Cl2, washed with H2O, brine, dried over Na2SO4, filtered and the filtrate was concentrated to provide (2-(difluoromethoxy)naphthalen-1-yl)methyl methanesulfonate (342 mg) as a brown oil that was used without further purification.

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후처리

  1. washwashed with H2O, brine
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-819f8b51e3b149dd92b243fa63041997
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394263B2

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