Methyl 3-(3-benzyloxycarbonyl-4-methoxyphenyl)-2,2-dimethylpropanoate → Methyl 3-(3-carboxy-4-methoxyphenyl)-2,2-dimethylpropanoate

HRID 1634525노트

반응식

HRID 1634525 반응식
C([O:8][C:9]([C:11]1[CH:12]=[C:13]([CH2:19][C:20]([CH3:26])([CH3:25])[C:21]([O:23][CH3:24])=[O:22])[CH:14]=[CH:15][C:16]=1[O:17][CH3:18])=[O:10])C1C=CC=CC=1>C(O)C.O1CCCC1.[Pd]>[C:9]([C:11]1[CH:12]=[C:13]([CH2:19][C:20]([CH3:26])([CH3:25])[C:21]([O:23][CH3:24])=[O:22])[CH:14]=[CH:15][C:16]=1[O:17][CH3:18])([OH:10])=[O:8]

참가 물질

5

반응물 1

HCID 11057401Methyl 3-(3-benzyloxycarbonyl-4-methoxyphenyl)-2,2-dimethylpropanoate

생성물 1

HCID 10923463Methyl 3-(3-carboxy-4-methoxyphenyl)-2,2-dimethylpropanoate수율 125.2%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 3-(3-benzyloxycarbonyl-4-methoxyphenyl)-2,2-dimethylpropanoate (310 mg, 0.870 mmol) was dissolved in 7 ml of mixed solvent of ethanol with tetrahydrofuran at a ratio of 1:1, 10% palladium on activated carbon (20 mg) was added thereto, and normal pressure hydrogenation was conducted for 5 hours. After completion of the reaction, catalyst was filtered and the filtrate was concentrated to obtain 290 mg (90%) of the title compound as a colorless oil.

후처리

  1. additionwas added
  2. customAfter completion of the reaction, catalyst
  3. filtrationwas filtered
  4. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-bb04c12890e043c1b6d70ca54ffb507e
출처 데이터셋
uspto-grants-2003_01
특허 번호
US06506797B1

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