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Tetrahydrofuran → HCID 178499559, 화합물

HRID 1295224
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HRID 1295224 반응식
C([O:8][C:9]1[C:13]([CH2:14][C:15]([O:17][CH3:18])=[O:16])=[CH:12][N:11]([CH3:19])[N:10]=1)C1C=CC=CC=1.O1CCCC1>[C].[Pd].C(O)C>[OH:8][C:9]1[C:13]([CH2:14][C:15]([O:17][CH3:18])=[O:16])=[CH:12][N:11]([CH3:19])[N:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8028TetrahydrofuranHCID 69427071methyl 3-benzyloxy-1-methyl-1H-pyrazol-4-ylacetate

생성물 1

HCID 178499559HCID 178499559, 화합물수율 79.4%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

A mixture of methyl 3-benzyloxy-1-methyl-1H-pyrazol-4-ylacetate (12.2 g), 5% palladium-carbon (25.0 g), tetrahydrofuran (100 ml) and ethanol (100 ml) was stirred under hydrogen atmosphere for 5 hrs. Palladium-carbon was filtered off and the filtrate was concentrated to give methyl 3-hydroxy-1-methyl-1H-pyrazol-4-ylacetate (6.33 g, yield 79%) as colorless crystals. The crystals were recrystallized from tetrahydrofuran-hexane. melting point: 118–119° C.

후처리

  1. filtrationPalladium-carbon was filtered off
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-0300f95395d24c76b164716c37219bad
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241785B2

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