Hydrazine hydrate (1:1) → Benzyl 4-(hydroxyamino)benzoate

HRID 1599466

반응식

HRID 1599466 반응식
O.NN.[N+:4]([C:7]1[CH:22]=[CH:21][C:10]([C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:12])=[CH:9][CH:8]=1)([O-])=[O:5]>[Rh].O1CCCC1>[OH:5][NH:4][C:7]1[CH:22]=[CH:21][C:10]([C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:12])=[CH:9][CH:8]=1

참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 84647Phenylmethyl 4-nitrobenzoate

생성물 1

HCID 18928833Benzyl 4-(hydroxyamino)benzoate

시약·촉매·용매 2

HCID 23948Rhodium촉매HCID 8028Tetrahydrofuran용매

실험 절차

Hydrazine hydrate (containing 55% hydrazine, 1.5 mL, 26.25 mmol, 1.05 equiv.) was added dropwise over 1 minute to a mixture containing benzyl 4-nitrobenzoate (Brewster, J. H.; Ciotti, C. J., Jr. J. Am. Chem. Soc. 1955, 77, 6214; 6.43 g, 25 mmole, 1 equiv.), 5% rhodium on carbon (wet, 625 mg), and tetrahydrofuran (50 ml) at 0° C. under argon. When the addition was complete, the mixture was warmed to room temperature, stirred for 4 hours, and then was filtered through Celite®. Concentration of the filtrate gave crude benzyl 4-(hydroxyamino)benzoate as a yellow oil which was used without further purification. Pure benzyl 4-(hydroxyamino)benzoate, obtained from a separate preparation by silica gel chromatography (30% ethyl acetate/toluene) was used for characterization purposes: TLC(30% ethyl acetate/toluene) Rf 0.52; 1H NMR (250 MHz, CDCl3) δ 7.99 (d, J=8.6 Hz, 2 H), 7.26-7.55 (m, 5 H), 6.97 (d, J=8.6 Hz, 2H), 5.33 (s, 2H); IR (CHCl3) 3550, 3315, 1703, 1606, 1273, 1169, 1101, 693 cm-1 ; MS(DC/NH3) 261.2 (M+NH4)+, 245.2 (M+MH4 -16)+, 228.1 (M+H-16)+.

후처리

  1. additionWhen the addition
  2. filtrationwas filtered through Celite®
  3. customConcentration of the filtrate gave crude benzyl 4-(hydroxyamino)benzoate as a yellow oil which
  4. customwas used without further purification

출처 및 근거

ORD 기록
ord-9e832134237844ac903c04e6a71a3348
출처 데이터셋
uspto-grants-1998_04
특허 번호
US05741804

연결된 노트

불러오는 중…