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p-Toluenesulfonic acid monohydrate → Benzo[b]thiophene-5-acetic acid

HRID 2390962
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HRID 2390962 반응식
[S:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10](C(O)=O)[C:11]([OH:13])=[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(C)=CC=CC=1>[S:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][C:11]([OH:13])=[O:12])=[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 576150412-(1-Benzothiophen-5-yl)malonic acid

생성물 1

HCID 11469582Benzo[b]thiophene-5-acetic acid수율 98.3%

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

To xylene (2 mL) suspension of 0.10 g of 2-(1-benzothiophen-5-yl)malonic acid was added 4 mg of p-toluenesulfonic acid monohydrate, which was then refluxed for 1 hour. The solvent was distilled off under reduced pressure, and to the resultant residue was added cyclohexane. The precipitate was collected by filtration to provide 0.08 g of 2-(1-benzothiophen-5-yl)acetic acid as white solid form.

후처리

  1. temperaturewas then refluxed for 1 hour
  2. distillationThe solvent was distilled off under reduced pressure
  3. additionto the resultant residue was added cyclohexane
  4. filtrationThe precipitate was collected by filtration

출처 및 근거

ORD 기록
ord-d153fde41fd2405e971d797d8234b1e8
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273902B2

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