Реакция #632002

ord-72a0928ff62c48d3bb640f42944f5ac1

Уравнение реакции

C=C[C@@H]1C[C@]1(NC(=O)OC(C)(C)C)C(=O)O
N-Boc-(1R,2S)-1-amino-2-vinylcyclopropane carboxylic acid
CCCCCC.CCOC(C)=O
ethyl acetate hexane
C=[N+]=[N-]
diazomethane
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)C[C@H]1C1CC1
(1R,2S)—N-Boc-1-amino-2-cyclopropylcyclopropane carboxylic acid ethyl ester
Выход 78.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe excess diazomethane was removed
  2. 2
    Концентрированиеthe resulting solution was concentrated by rotary evaporation
  3. 3
    Другоеto give the crude product

Методика

A solution of N-Boc-(1R,2S)-1-amino-2-vinylcyclopropane carboxylic acid (255 mg, 1.0 mmol) in diethyl ether (10 mL) was treated with palladium acetate (5 mg, 0.022 mmol). The orange/red solution was placed under a nitrogen atmosphere. An excess of diazomethane in diethyl ether was added dropwise over the course of 1 hour. The resulting solution was stirred at room temperature for 18 hours. The excess diazomethane was removed using a stream of nitrogen and the resulting solution was concentrated by rotary evaporation to give the crude product. Flash chromatography (10% ethyl acetate/hexane) provided 210 mg (78%) of (1R,2S)—N-Boc-1-amino-2-cyclopropylcyclopropane carboxylic acid ethyl ester as a colorless oil. LC-MS (retention time: 2.13, similar to method A except: gradient time 3 minutes, Xterra MS C18 S7 3.0×50 mm column), MS m/e 270 (M++1).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07935670B2uspto-grants-2011_05