Ethyl 2,5-dichlorothiophene-3-carboxylate → 2,5-Dichlorothiophene-3-carboxylic acid

HRID 357752노트

반응식

HRID 357752 반응식
C([O:3][C:4]([C:6]1[CH:10]=[C:9]([Cl:11])[S:8][C:7]=1[Cl:12])=[O:5])C>C(O)C.O1CCCC1.[OH-].[Na+]>[Cl:12][C:7]1[S:8][C:9]([Cl:11])=[CH:10][C:6]=1[C:4]([OH:5])=[O:3]

참가 물질

5

실험 절차

3-Thiophenecarboxylic acid ethyl ester (1.56 g) was dissolved in acetonitrile (30 ml), and sulfuryl chloride (5.36 g) was added. The mixture was stirred at room temperature for 4 hours, and 10% aqueous sodium thiosulfate (100 ml) was added. The mixture was stirred for 15 minutes and extracted with diethyl ether. The extract was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 2,5-dichloro-3-thiophenecarboxylic acid ethyl ester (2.3 g). 2,5-Dichloro-3-thiophenecarboxylic acid ethyl ester (2.25 g) was dissolved in a mixture of ethanol (10 ml) and tetrahydrofuran (10 ml), and 1N aqueous sodium hydroxide (20 ml) was added. The mixture was stirred at room temperature for 2 hours and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 2,5-dichloro-3-thiophenecarboxylic acid (1.89 g) as crystals.

후처리

  1. additionwas added
  2. washwashed with diethyl ether
  3. extractionextracted with ethyl acetate
  4. dry with materialThe extract was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-06e1362627214e568b548d6de13e678f
출처 데이터셋
uspto-grants-1998_11
특허 번호
US05840917

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