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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-Methoxy-N-methylbenzofuran-5-carboxamide → 2,3-Dihydro-benzofuran-5-carboxylic acid methoxy-methyl-amide

HRID 1671361
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인쇄 미리보기

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HRID 1671361 반응식
[CH3:1][O:2][N:3]([CH3:15])[C:4]([C:6]1[CH:7]=[CH:8][C:9]2[O:13][CH:12]=[CH:11][C:10]=2[CH:14]=1)=[O:5]>C(O)C.[Pd]>[CH3:1][O:2][N:3]([CH3:15])[C:4]([C:6]1[CH:7]=[CH:8][C:9]2[O:13][CH2:12][CH2:11][C:10]=2[CH:14]=1)=[O:5]
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참가 물질

4

반응물 1

HCID 59186071N-Methoxy-N-methylbenzofuran-5-carboxamide2회

생성물 1

HCID 591860532,3-Dihydro-benzofuran-5-carboxylic acid methoxy-methyl-amide

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution of benzofuran-5-carboxylic acid methoxy-methyl-amide (Intermediate P, 235 mg, 1.145 mmol) in ethanol (20 ml) is hydrogenated over 10% Pd on carbon (30×4 mm CatCart®) at 40° C. and 30 bar using the H-Cube Hydrogenator. After 6 hrs the reaction is complete and the reaction mixture is concentrated in vacuo to give an oil; MS m/z=208.1 [M+H]+; H NMR 400.13 MHz (CDCl3)-7.6 (1H, s), 7.55 (1H, d), 7.8 (1H, d), 4.6 (2H, t), 3.6 (3H, s), 3.35 (3H, s), 3.25 (2H, t).

후처리

  1. concentrationthe reaction mixture is concentrated in vacuo
  2. customto give an oil

출처 및 근거

ORD 기록
ord-680530ea05b944198daa0e1529f19d67
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994203B2

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