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Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 10154224, 화합물

HRID 279175
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HRID 279175 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:18])[C@@H:9]([O:11]C1CCCCO1)[CH3:10].C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1>C(O)C>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:18])[C@@H:9]([OH:11])[CH3:10]
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참가 물질

4

반응물 2

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 10264208HCID 10264208, 화합물

생성물 1

HCID 10154224HCID 10154224, 화합물수율 98.4%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
55 °C

실험 절차

(2S)-2′-Fluoro-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)propiophenone (25 g) was dissolved in ethanol (200 ml), to which pyridinium p-toluenesulfonate (1.28 g) was added. The reaction solution was stirred at 55° C. for 2.5 hours and then concentrated. The residue was subjected to silica gel chromatography (eluent: hexane/ethyl acetate=9/1 to 5/1) to give (2S)-2′-fluoro-2-hydroxypropiophenone (16.4 g) as a colorless oily substance.

후처리

  1. additionwas added
  2. concentrationconcentrated

출처 및 근거

ORD 기록
ord-66ae20787e1842d8aec3a220eeedb9d0
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06362206B1

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