Benzaldehyde → methyl 3-[(2E)-2-benzylidenehydrazinyl]thiophene-2-carboxylate

HRID 601214노트

반응식

HRID 601214 반응식
[NH:1]([C:3]1[CH:7]=[CH:6][S:5][C:4]=1[C:8]([O:10][CH3:11])=[O:9])[NH2:2].[CH:12](=O)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(O)C>[CH:12](=[N:2]/[NH:1][C:3]1[CH:7]=[CH:6][S:5][C:4]=1[C:8]([O:10][CH3:11])=[O:9])\[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

참가 물질

4

반응물 2

HCID 240BenzaldehydeHCID 2777595Methyl 3-Hydrazinothiophene-2-Carboxylate

생성물 1

HCID 12645679methyl 3-[(2E)-2-benzylidenehydrazinyl]thiophene-2-carboxylate수율 104.8%

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
25 °C

실험 절차

A solution of methyl 3-hydrazinothiophene-2-carboxylate (Maybridge technical grade, 2.0 g, 0.11 mol) in ethanol (250 mL) at 25° C. was reacted with a solution of benzaldehyde (12.32 g, 0.11 mol) in ethanol (100 mL). The mixture was stirred at 25° C. for 1.5 hours and concentrated to yield 30 g of a white solid. HPLC/MS show a single peak with retention time of 2.35 min. and a M+1 peak of 261. 1H NMR (300 MHz, CDCl3) δ ppm 3.85 (s, 3 H) 7.35 (m, 4 H) 7.64 (dd, J=8.09, 1.47 Hz, 2 H) 7.77 (s, 1 H) 10.10 (s, 1 H).

후처리

  1. concentrationconcentrated

출처 및 근거

ORD 기록
ord-28e24a5fdd3740b4b077cf28f8c4a483
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07902203B2

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