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Hydrochloric Acid → 6-(6-carboxybenzofuran-2-yl)-3,5-dimethyl-4-hydroxy-2H-pyran-2-one

HRID 1357210
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HRID 1357210 반응식
C([O:4][C:5]1[C:10]([CH3:11])=[C:9]([C:12]2[O:13][C:14]3[CH:20]=[C:19]([C:21]([O:23]C)=[O:22])[CH:18]=[CH:17][C:15]=3[CH:16]=2)[O:8][C:7](=[O:25])[C:6]=1[CH3:26])(=O)C.C([O-])([O-])=O.[K+].[K+].Cl>CO.O>[C:21]([C:19]1[CH:18]=[CH:17][C:15]2[CH:16]=[C:12]([C:9]3[O:8][C:7](=[O:25])[C:6]([CH3:26])=[C:5]([OH:4])[C:10]=3[CH3:11])[O:13][C:14]=2[CH:20]=1)([OH:23])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 185055404-acetyloxy-3,5-dimethyl-6-(6-(methoxycarbonyl)benzofuran-2-yl)-2H-pyran-2-one

생성물 1

HCID 546827716-(6-carboxybenzofuran-2-yl)-3,5-dimethyl-4-hydroxy-2H-pyran-2-one

시약·촉매·용매 2

HCID 887Methanol용매
HCID 962
Water
용매

실험 절차

A mixed solution of 4-acetyloxy-3,5-dimethyl-6-(6-(methoxycarbonyl)benzofuran-2-yl)-2H-pyran-2-one (85 mg) and K2CO3 (45 mg) in MeOH (5 ml) and H2O (1 ml) was stirred at room temperature for one hour, and then the reaction solution was rendered acidic with a 1 N hydrochloric acid aqueous solution and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (AcOEt/MeOH=5/1) to obtain 6-(6-carboxybenzofuran-2-yl)-3,5-dimethyl-4-hydroxy-2H-pyran-2-one.

후처리

  1. concentrationconcentrated under reduced pressure
  2. customThe residue was purified by silica gel column chromatography (AcOEt/MeOH=5/1)

출처 및 근거

ORD 기록
ord-2bf419492e794606a5eea80949e59d93
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06589984B1

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