tert-Butyl hydroperoxide → Ethyl 6-acetyl-2,3-dihydro-1,4-benzodioxine-2-carboxylate

HRID 1756026

반응식

HRID 1756026 반응식
[CH2:1]([C:3]1[CH:17]=[CH:16][C:6]2[O:7][CH:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:9][O:10][C:5]=2[CH:4]=1)[CH3:2].C([O:22]O)(C)(C)C>C(Cl)Cl.[O-2].[O-2].[O-2].[Cr+6]>[C:1]([C:3]1[CH:17]=[CH:16][C:6]2[O:7][CH:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:9][O:10][C:5]=2[CH:4]=1)(=[O:22])[CH3:2]

참가 물질

5

반응물 2

HCID 6410tert-Butyl hydroperoxideHCID 15210220Ethyl 6-ethyl-2,3-dihydro-1,4-benzodioxin-2-carboxylate

생성물 1

HCID 15210221Ethyl 6-acetyl-2,3-dihydro-1,4-benzodioxine-2-carboxylate수율 62%

시약·촉매·용매 2

HCID 10219390chromium (VI) trioxide촉매HCID 6344Dichloromethane용매2회

반응 조건

온도
0 °C

실험 절차

Add 2 g (8.5 mmol) of ethyl 6-ethyl-2,3-dihydro-1,4-benzodioxin-2-carboxylate dissolved in 5 cm3 of anhydrous methylene chloride to a mixture at 0° C. of 0.042 g (0.42 mmol) of chromium trioxide and 5.35 g (59.3 mmol) of 70% tert-butyl hydroperoxide in 30 cm3 of methylene chloride. Stir for 2 hours at 0° C. and then for 72 hours at room temperature. The crude product obtained by concentrating to dryness is purified by chromatography on a silica column (eluant: methylene chloride). Ethyl 6-acetyl-2,3-dihydro-1,4-benzodioxin-2-carboxylate is thereby obtained in a yield of 62%. Melting point: 60° C.

후처리

  1. waitfor 72 hours at room temperature
  2. customThe crude product obtained
  3. concentrationby concentrating to dryness
  4. customis purified by chromatography on a silica column (eluant: methylene chloride)

출처 및 근거

ORD 기록
ord-d687941ae6164db7abd9fc2137968029
출처 데이터셋
uspto-grants-1995_08
특허 번호
US05439909

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