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Water → Sodium 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate

HRID 589287
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반응식

HRID 589287 반응식
[F:1][C:2]([F:17])([F:16])[C:3]1[CH:15]=[CH:14][C:6]2[S:7][C:8]([C:10]([O:12]C)=[O:11])=[CH:9][C:5]=2[CH:4]=1.C(=O)([O-])[O-].[Na+:22].[Na+].O>CO>[F:17][C:2]([F:1])([F:16])[C:3]1[CH:15]=[CH:14][C:6]2[S:7][C:8]([C:10]([O-:12])=[O:11])=[CH:9][C:5]=2[CH:4]=1.[Na+:22]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 10340Sodium CarbonateHCID 14779565-Trifluoromethyl-benzo[b]thiophene-2-carboxylic acid methyl ester

생성물 1

HCID 70982299Sodium 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate수율 99%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
80 °C
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실험 절차

A mixture of 5.00 g of methyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, 4.00 g of sodium carbonate, 20 ml of water and 60 ml of methanol was stirred at 80° C. for 3 hours. The reaction mixture was cooled to room temperature, and then concentrated under reduced pressure. The residue was recrystallized from water to obtain 5.10 g of sodium 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate (hereinafter referred to as “the present compound 5”).

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. customThe residue was recrystallized from water

출처 및 근거

ORD 기록
ord-858cb6d0ac58419aa5439eb973b517bd
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09232792B2

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