4-Hydroxybenzoic Acid → N-(Benzyloxy)-4-hydroxybenzamide

HRID 2375214노트

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HRID 2375214 반응식
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[CH:4][CH:3]=1.Cl.[CH2:12]([O:19][NH2:20])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.Cl.CN(C)CCCN=C=NCC.O>CN(C)C1C=CN=CC=1.ClCCl>[CH2:12]([O:19][NH:20][C:6](=[O:8])[C:5]1[CH:4]=[CH:3][C:2]([OH:1])=[CH:10][CH:9]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

참가 물질

7

실험 절차

To a mixture of 4-hydroxybenzoic acid (E18) (0.424 g, 3.07 mmol), O-benzylhydroxylamine hydrochloride (E19) (0.490 g, 3.07 mmol), and 4-dimethylaminopyridine (0.414 g, 3.39 mmol) in dichloromethane (30 ml) under argon atmosphere, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.643 g, 3.35 mmol) was added and the resultant mixture was stirred at room temperature for 5 hours. The reaction mixture was poured into a mixture of saturated NaH2PO4 (30 ml) and water (70 ml), and extracted with ethyl acetate (2×75 ml). The extract was washed with a mixture of saturated NaH2PO4 (15 ml) and water (35 ml), brine (50 ml), and dried (MgSO4). The solvent was evaporated and the residue was chromatographed on silicagel (50 g) with benzene-ethyl acetate-acetic acid (75:25:1, 100 ml) and benzene-ethyl acetate-acetic acid (50:50:1, 300 ml) as eluents to give the title compound (0.338 g, 45%) as a white solid. 1H NMR (DMSO-d6, HMDSO), δ: 4.88 (2H, s); 6.79 (2H, d, J=8.8 Hz); 7.23-7.55 (5H, m); 7.59 (2H, d, J=8.8 Hz); 10.02 (1H, br s); 11.48 (1H, s).

후처리

  1. extractionextracted with ethyl acetate (2×75 ml)
  2. washThe extract was washed with a mixture of saturated NaH2PO4 (15 ml) and water (35 ml), brine (50 ml)
  3. dry with materialdried (MgSO4)
  4. customThe solvent was evaporated
  5. customthe residue was chromatographed on silicagel (50 g) with benzene-ethyl acetate-acetic acid (75:25:1, 100 ml) and benzene-ethyl acetate-acetic acid (50:50:1, 300 ml) as eluents

출처 및 근거

ORD 기록
ord-e3418371b5594e7e9dfb2a8155581291
출처 데이터셋
uspto-grants-2008_12
특허 번호
US07465719B2

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