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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Lithium Hydroxide → 5-Chloro-3-(trifluoromethyl)-1-benzothiophene-2-carboxylic acid

HRID 2038410
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인쇄 미리보기

반응식

HRID 2038410 반응식
[Cl:1][C:2]1[CH:18]=[CH:17][C:5]2[S:6][C:7]([C:13]([O:15]C)=[O:14])=[C:8]([C:9]([F:12])([F:11])[F:10])[C:4]=2[CH:3]=1.[Li+].[OH-]>C1COCC1.CO.O>[Cl:1][C:2]1[CH:18]=[CH:17][C:5]2[S:6][C:7]([C:13]([OH:15])=[O:14])=[C:8]([C:9]([F:12])([F:11])[F:10])[C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 59625756HCID 59625756, 화합물

생성물 1

HCID 591641865-Chloro-3-(trifluoromethyl)-1-benzothiophene-2-carboxylic acid

시약·촉매·용매 1

HCID 21892291Methanol tetrahydrofuran water용매

실험 절차

A mixture of compound 11e (390 mg, 1.33 mmol) and LiOH (159 mg, 6.65 mmol) in THF/MeOH/H2O (4/4/4 mL) was stirred for 4 h. The reaction was concentrated under reduced pressure and then water was added to the residue. The aqueous mixture was acidified with 1N HCl to pH ˜4. A white precipitate was filtered and washed with water and Et2O. The crude product was dried under vacuum to give compound 11f which was used without purification.

후처리

  1. concentrationThe reaction was concentrated under reduced pressure
  2. additionwater was added to the residue
  3. filtrationA white precipitate was filtered
  4. washwashed with water and Et2O
  5. dry with materialThe crude product was dried under vacuum

출처 및 근거

ORD 기록
ord-e9ef8874be88478c8fa218fbd79bf920
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08575363B2

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