反応 #172573

ord-95cc40b53c754e7d88aa833f6e43ab20

反応方程式

CCOC(=O)c1ccccc1O
ethyl 2-hydroxybenzoate
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)O
2-(tert-butoxycarbonylamino)-3-phenylpropanoic acid
CCN=C=NCCCN(C)C
EDCI
CN(C)c1ccccn1
dimethylaminopyridine
CCOC(=O)c1ccccc1OC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C
ethyl 2-(2-(tert-butoxycarbonylamino)-3-phenylpropanoyloxy)benzoate
収率 96.7%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他partitioned between CH2Cl2 and brine
  2. 2
    抽出The aqueous layer was extracted with CH2Cl2
  3. 3
    乾燥the combined organic extracts were dried over MgSO4
  4. 4
    その他The crude material was purified by silica gel chromatography (0-10% MeOH/CH2Cl2)

実験手順

To a solution of ethyl 2-hydroxybenzoate (0.5 g, 3.0 mmol) in CH2Cl2 (8 mL) was added 2-(tert-butoxycarbonylamino)-3-phenylpropanoic acid (0.8 g, 3.0 mmol), EDCI (0.63 g, 3.3 mmol) and dimethylaminopyridine (0.037 g, 0.3 mmol). The reaction was stirred (RT, 3 h) and then partitioned between CH2Cl2 and brine. The aqueous layer was extracted with CH2Cl2 and the combined organic extracts were dried over MgSO4. The crude material was purified by silica gel chromatography (0-10% MeOH/CH2Cl2) to afford ethyl 2-(2-(tert-butoxycarbonylamino)-3-phenylpropanoyloxy)benzoate (1.2 g). Mass calculated for C235H27NO6=413.46; found: [M+Na]+=437.1.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08846972B2uspto-grants-2014_09