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Sodium Hydroxide → 1-Methylsulfonyl-2-trifluoromethoxybenzene

HRID 967650
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반응식

HRID 967650 반응식
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][C:10]([F:13])([F:12])[F:11].ClC1C=C(C=CC=1)C(OO)=[O:19].[OH-:25].[Na+]>C(Cl)Cl>[CH3:1][S:2]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][C:10]([F:11])([F:12])[F:13])(=[O:19])=[O:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 70297m-Chloroperbenzoic acidHCID 27815671-(Methylthio)-2-(trifluoromethoxy)benzene

생성물 1

HCID 223110911-Methylsulfonyl-2-trifluoromethoxybenzene

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

1-Methylsulfanyl-2-trifluoromethoxybenzene (15.0 g, 72 mmol) was dissolved in DCM (200 mL) and m-chloroperoxybenzoic acid (39.0 g, 216 mmol) was added in small portions during 30 min. The reaction mixture was then allowed to stand overnight. DCM (200 mL) was added followed by slow addition of sodium hydroxide (2 N, 200 mL). The organic phase was separated and washed with sodium hydroxide (2 N, 3×150 mL), dried (magnesium sulphate) and concentrated in vacuo to give 15.8 g of 1-methylsulfonyl-2-trifluoromethoxybenzene

후처리

  1. customThe organic phase was separated
  2. washwashed with sodium hydroxide (2 N, 3×150 mL)
  3. dry with materialdried (magnesium sulphate)
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-cfb715f50ddc4d40b9d7c865345ad812
출처 데이터셋
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06953812B2

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