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Sodium Hydroxide → 2-Chloro-5-(2-methyl-1,3-thiazol-4-yl)benzoic acid

HRID 1988391
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반응식

HRID 1988391 반응식
C[O:2][C:3](=[O:17])[C:4]1[CH:9]=[C:8]([C:10]2[N:11]=[C:12]([CH3:15])[S:13][CH:14]=2)[CH:7]=[CH:6][C:5]=1[Cl:16].[OH-].[Na+]>C(O)(C)(C)C>[Cl:16][C:5]1[CH:6]=[CH:7][C:8]([C:10]2[N:11]=[C:12]([CH3:15])[S:13][CH:14]=2)=[CH:9][C:4]=1[C:3]([OH:17])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 588181942-Chloro-5-(2-methyl-thiazol-4-yl)-benzoic acid methyl ester

생성물 1

HCID 184386562-Chloro-5-(2-methyl-1,3-thiazol-4-yl)benzoic acid수율 69%

시약·촉매·용매 1

HCID 6386tert-Butanol용매

실험 절차

A mixture of 2-chloro-5-(2-methyl-thiazol-4-yl)-benzoic acid methyl ester (10 mg, 0.04 mmol) and sodium hydroxide (80 μL, 1M aqueous, 0.08 mmol) in tert-butanol (1 mL) was stirred at room temperature for 3 d. The mixture was concentrated to dryness in vacuo, dissolved in water (5 mL), acidified to pH 6 (1M HCl) and extracted with ethyl acetate. The combined organic layers were washed with water, and brine, dried over sodium sulfate, filtered and concentrated in vacuo to afford the title compound (7 mg).

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후처리

  1. concentrationThe mixture was concentrated to dryness in vacuo
  2. dissolutiondissolved in water (5 mL)
  3. extractionextracted with ethyl acetate
  4. washThe combined organic layers were washed with water, and brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3823e27843974f118c7eedad789552a1
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07553972B2

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