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p-Toluenesulfonic acid monohydrate → 7-Methoxy-2-(tetrahydrofuran-2-yl)-benzofuran

HRID 1282030
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인쇄 미리보기

반응식

HRID 1282030 반응식
[CH3:1][O:2][C:3]1[C:11]2[O:10][C:9]([CH:12]([OH:17])[CH2:13][CH2:14][CH2:15]O)=[CH:8][C:7]=2[CH:6]=[CH:5][CH:4]=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>ClCCl>[CH3:1][O:2][C:3]1[C:11]2[O:10][C:9]([CH:12]3[CH2:13][CH2:14][CH2:15][O:17]3)=[CH:8][C:7]=2[CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 184236471-(7-Methoxybenzofuran-2-yl)-butane-1,4-diol

생성물 1

HCID 184236387-Methoxy-2-(tetrahydrofuran-2-yl)-benzofuran수율 71.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 1-(7-methoxybenzofuran-2-yl)-butane-1,4-diol (0.88 g) was treated with p-toluenesulfonic acid monohydrate (10 mg) and 3 Å molecular sieves in dichloromethane (10 ml) at ambient temperature. After stirring for 1 hour the solvent was removed in vacuo. The residue was purified by column chromatography on silica eluting with 20% ethyl acetate in hexane to give the title compound as a yellow oil (0.58 g).

후처리

  1. customwas removed in vacuo
  2. customThe residue was purified by column chromatography on silica eluting with 20% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-eb973e94b9224c61b7066eccc23f5b70
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06455561B1

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