反応 #632013

ord-2746782059b54ffa914bcd8aa0ea477b

反応方程式

CC(C)(C)NC(=O)O.COCC1(S(N)(=O)=O)CC1
1-methoxymethylcyclopropylsulfonylamine tert-butylcarbamate
COCC1(S(N)(=O)=O)CC1
desired product
COCC1(S(N)(=O)=O)CC1
1-methoxymethylcyclopropysulfonamide

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The solvent was removed in vacuo
  2. 2
    その他the residue purified by column chromatography over 80 g of SiO2 (eluting with 0% to 60% ethyl acetate/hexanes)

実験手順

A solution of 1-methoxymethylcyclopropylsulfonylamine tert-butylcarbamate (1.14 g, 4.30 mmol) was dissolved in a solution of 50% TFA/dichloromethane (30 mL) and was stirred at room temperature for 16 hours. The solvent was removed in vacuo and the residue purified by column chromatography over 80 g of SiO2 (eluting with 0% to 60% ethyl acetate/hexanes) to provide the desired product as a white solid (0.55 g, 77% overall over two steps): 1H NMR (CDCl3) δ 0.95 (m, 2H), 1.44 (m, 2H), 3.36 (s, 3H), 3.65 (s, 2H), 4.85 (s, 2H); 13C NMR (CDCl3) δ 11.17, 40.87, 59.23, 74.80; LRMS m/z 183 (M++NH4).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07935670B2uspto-grants-2011_05