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p-Toluenesulfonic acid monohydrate → 2-(1-Benzothiophen-5-yl)malonic acid

HRID 2390961
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인쇄 미리보기

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HRID 2390961 반응식
[S:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10]([C:18]([O:20]C(C)(C)C)=[O:19])[C:11]([O:13]C(C)(C)C)=[O:12])=[CH:9][C:4]=2[CH:3]=[CH:2]1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[S:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10]([C:11]([OH:13])=[O:12])[C:18]([OH:20])=[O:19])=[CH:9][C:4]=2[CH:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 58239411Di(tert-butyl)2-(1-benzothiophen-5-yl)malonate

생성물 1

HCID 576150412-(1-Benzothiophen-5-yl)malonic acid수율 82.6%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To toluene (2.5 mL) solution of 0.25 g of di(tert-butyl) 2-(1-benzothiophen-5-yl)malonate was added 0.01 g of p-toluenesulfonic acid monohydrate, which was then refluxed for 1 hour. After cooling the reaction mixture, the precipitate was collected by filtration to provide 0.14 g of 2-(1-benzothiophen-5-yl)malonic acid as white solid form.

후처리

  1. temperaturewas then refluxed for 1 hour
  2. temperatureAfter cooling the reaction mixture
  3. filtrationthe precipitate was collected by filtration

출처 및 근거

ORD 기록
ord-054bd898c26843d5af008bce44cc61f2
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273902B2

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