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HCID 66722704, 화합물 → Methyl 3-carbamoyl-4-hydroxybenzoate

HRID 1639533
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HRID 1639533 반응식
C([O:8][C:9]1[CH:18]=[CH:17][C:12]([C:13]([O:15][CH3:16])=[O:14])=[CH:11][C:10]=1[C:19](=[O:21])[NH2:20])C1C=CC=CC=1.[H][H]>CO.[Pd]>[C:19]([C:10]1[CH:11]=[C:12]([CH:17]=[CH:18][C:9]=1[OH:8])[C:13]([O:15][CH3:16])=[O:14])(=[O:21])[NH2:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 66722704HCID 66722704, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 10607886Methyl 3-carbamoyl-4-hydroxybenzoate수율 96.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

Hydrogenolysis is effected by dissolving 1.2 gm (4.2 mmol) of methyl 4-benzyloxy-3-carbamoylbenzoate in 60 mL of methanol (warmed to effect solution), adding 1 gm of 10% Pd/C (50% water) catalyst, and stirring under 48 psi of hydrogen overnight at room temperature. The reaction mixture is filtered, and the catalyst is repeatedly washed with 10% MeOH/DCM. The combined filtrates are evaporated to dryness to give 0.79 gm (4.05 mmol, 96% yield) of methyl 3-carbamoyl-4-hydroxybenzoate.

후처리

  1. filtrationThe reaction mixture is filtered
  2. washthe catalyst is repeatedly washed with 10% MeOH/DCM
  3. customThe combined filtrates are evaporated to dryness

출처 및 근거

ORD 기록
ord-5657a81bc4a645d7b86e8a8ae20acb10
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08110570B2

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