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m-Chloroperbenzoic acid → 2-Fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile

HRID 839
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HRID 839 반응식
[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10][C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=2)[C:3]=1[C:4]#[N:5].ClC1C=CC=C(C(OO)=[O:27])C=1.S(=O)(O)[O-].[Na+]>O>[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=2)=[O:27])[C:3]=1[C:4]#[N:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 70297m-Chloroperbenzoic acid2회HCID 107064062-Fluoro-6-[(3-methoxyphenyl)thio]benzonitrileHCID 23665763Sodium Bisulfite

생성물 1

HCID 107787732-Fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a solution of 2 g (7.7 mmol) of 2-fluoro-6-[(3-methoxyphenyl)thio]benzonitrile (Example 13) was added portionwise 1.6 g (9.3 mmol) of m-chloroperbenzoic acid. The resultant mixture was stirred for 24 h. Additional 0.16 g of m-chloroperbenzoic acid was added and the resultant mixture was stirred for 15 min. Excess sodium bisulfite was added, followed by water. The H2O solution was extracted with EtOAc. After drying over MgSO4 and solvent removal, the resultant crude product was purified by flash column chromatography on silica gel with methylene chloride as the eluent. This resulted in 1.7 g of 2-fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile as a solid: mp 103°-111° C.

후처리

  1. extractionThe H2O solution was extracted with EtOAc
  2. dry with materialAfter drying over MgSO4 and solvent removal
  3. customthe resultant crude product was purified by flash column chromatography on silica gel with methylene chloride as the eluent
  4. customThis resulted in 1.7 g of 2-fluoro-6-[(3-methoxyphenyl)sulfinyl]benzonitrile as a solid

출처 및 근거

ORD 기록
ord-f52f628e55bf48349560d5f7350120df
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05723452

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