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Ethanol → 2-(Benzo[b]thiophen-3-yl)ethanol

HRID 502502
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인쇄 미리보기

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HRID 502502 반응식
[S:1]1[CH:5]=[C:4]([CH2:6][C:7](O)=[O:8])[C:3]2[CH:10]=[CH:11][CH:12]=[CH:13][C:2]1=2.[Li].C(O)C>O1CCCC1>[S:1]1[CH:5]=[C:4]([CH2:6][CH2:7][OH:8])[C:3]2[CH:10]=[CH:11][CH:12]=[CH:13][C:2]1=2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 70799Benzo[b]thiophene-3-acetic acidHCID 3028194Lithium

생성물 1

HCID 158522062-(Benzo[b]thiophen-3-yl)ethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
60 °C

실험 절차

A solution of benzo[b]thiophen-3-yl-acetic acid (6.0 g, 31.2 mmol) in 40 ml of tetrahydrofuran was added dropwise at RT to a suspension of lithium alanate (1.54 g, 41 mmol) in 35 ml of tetrahydrofuran. The mixture was stirred for 60 minutes at 60° C., and then excess alanate was hydrolysed with ethanol. The mixture was suction-filtered over Kieselguhr and the solvent was removed in vacuo. The product was obtained in the form of a yellowish oil in a yield of 5.1 g (92%).

후처리

  1. filtrationThe mixture was suction-filtered over Kieselguhr
  2. customthe solvent was removed in vacuo
  3. customThe product was obtained in the form of a yellowish oil in a yield of 5.1 g (92%)

출처 및 근거

ORD 기록
ord-7d496dbea50649b3ba257d028bad7c01
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07776848B2

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