Benzyl Bromide → ethyl 1-benzyl-1H-pyrazole-4-carboxylate

HRID 64300

반응식

HRID 64300 반응식
[NH:1]1[CH:5]=[C:4]([C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH:3]=[N:2]1.C([O-])([O-])=O.[K+].[K+].[CH:17]1[CH:22]=[CH:21][C:20]([CH2:23]Br)=[CH:19][CH:18]=1>CC#N>[CH2:23]([N:1]1[CH:5]=[C:4]([C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH:3]=[N:2]1)[C:20]1[CH:21]=[CH:22][CH:17]=[CH:18][CH:19]=1

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 142179ethyl 1H-pyrazole-4-carboxylate

생성물 1

HCID 15237993ethyl 1-benzyl-1H-pyrazole-4-carboxylate수율 92.1%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a mixture of ethyl 1H-pyrazole-4-carboxylate (35.0 g, 250 mmol) and K2CO3 (69.0 g, 500 mmol) in CH3CN (250 mL) was added BnBr (42.7 g, 250 mmol). The mixture was stirred at RT for 18 h and concentrated. The residue was suspended in EA (500 mL), washed with water (200 mL×2), dried over Na2SO4 and concentrated to give the desired compound as a white solid (53.0 g, 91.2%). 1H NMR (DMSO-d6) δ 8.46 (s, 1H), 7.88 (s, 1H), 7.41-7.19 (m, 5H), 5.37 (s, 2H), 4.21 (q, 2H, J=5.4 Hz), 1.25 (t, 3H, J=5.4 Hz). MS (ESI) m/e [M+1]+ 231.0.

후처리

  1. concentrationconcentrated
  2. washwashed with water (200 mL×2)
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1e4b71ac9bba4479892d1bf30d9cf41c
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09447106B2

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