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Sodium Hydroxide → 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid

HRID 1926612
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HRID 1926612 반응식
[C:1]([C:3]1[C:4]([I:15])=[C:5]([C:10]([O:12]CC)=[O:11])[S:6][C:7]=1[S:8][CH3:9])#[N:2].[OH-].[Na+]>O1CCCC1.O>[C:1]([C:3]1[C:4]([I:15])=[C:5]([C:10]([OH:12])=[O:11])[S:6][C:7]=1[S:8][CH3:9])#[N:2]
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 40152061Ethyl 4-cyano-3-iodo-5-(methylthio)thiophene-2-carboxylate

생성물 1

HCID 580228624-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid수율 80%

시약·촉매·용매 2

HCID 962Water용매2회HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of ethyl 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylate (3.40 g, 10 mmol) in tetrahydrofuran (80 mL) and water (16 mL) was added a solution of 1.00M sodium hydroxide in water (30 mL). The solution was allowed to stir overnight. The reaction was quenched with a solution of 1N hydrogen chloride in water (50 mL) and diluted with water (400 mL). The resultant precipitate was filtered, washed with water (2×100 mL) and dried in a vacuum oven to give 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid (2.6 g, 79%) as a white solid. LCMS: (FA) ES+ 326. 1H NMR (400 MHz, d6-DMSO) δ: 14.1-13.8 (bs, 1H), 2.75 (s, 3H).

후처리

  1. customThe reaction was quenched with a solution of 1N hydrogen chloride in water (50 mL)
  2. additiondiluted with water (400 mL)
  3. filtrationThe resultant precipitate was filtered
  4. washwashed with water (2×100 mL)
  5. customdried in a vacuum oven

출처 및 근거

ORD 기록
ord-b7abdbdcd8854f438da08585f866262f
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08183240B2

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