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Methyl 2-(3-bromophenyl)acetate → (3-Bromophenyl)(pyridin-4-ylsulfanyl)acetic acid methyl ester

HRID 572896
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HRID 572896 반응식
C[SH+](C)=O.[CH3:5][O:6][C:7](=[O:16])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([Br:15])[CH:10]=1.[SH:17][C:18]1[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=1>ClC(Cl)C>[CH3:5][O:6][C:7](=[O:16])[CH:8]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([Br:15])[CH:10]=1)[S:17][C:18]1[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=1
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참가 물질

5

반응물 3

HCID 11746402Methyl 2-(3-bromophenyl)acetateHCID 22345572DimethylsulfoxoniumHCID 178418431pyridine-4-thiol

생성물 1

HCID 66836016(3-Bromophenyl)(pyridin-4-ylsulfanyl)acetic acid methyl ester

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매

실험 절차

To a solution of dimethylsulfoxonium ylide and 3-bromophenylacetic acid methyl ester (example 530E, 3 g) in dichloroethane (50 mL) are added 4-mercaptopyridine (2 equivalents) and [Ir(COD)Cl]2 (20 mg). The reaction mixture is refluxed overnight then concentrated to dryness under reduced pressure. The residue is purified by chromatography on silica gel (heptane/ethyl acetate 1/1) to give (3-Bromophenyl)(pyridin-4-ylsulfanyl)acetic acid methyl ester. 1H NMR: 8.50-8.35 (m, 2H), 7.68 (s, 1H), 7.55-7.45 (m, 2H), 7.35-7.20 (m, 1H), 7.20-7.05 (m, 2H), 5.08 (s, 1H), 3.77 (s, 3H).

후처리

  1. temperatureThe reaction mixture is refluxed overnight
  2. concentrationthen concentrated to dryness under reduced pressure
  3. customThe residue is purified by chromatography on silica gel (heptane/ethyl acetate 1/1)

출처 및 근거

ORD 기록
ord-25ec873f700c400386d34277e139be35
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029357B2

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