반응 #46078

ord-a44c3cd92f3e4d0d94826e01a47828e8

반응 방정식

CC(C)(C)NS(=O)(=O)C1(C)CC1
N-tert-Butyl-(1-methyl)cyclopropylsulfonamide
COC(=O)c1ccccc1
methyl benzoate
CC(C)(C)NS(=O)(=O)C1(C(=O)c2ccccc2)CC1
N-tert-Butyl-(1-benzoyl)cyclopropyl-sulfonamide
수율 66.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타This compound was obtained in 66% yield
  2. 2
    기타The compound was purified by column chromatography over SiO2 using 30% to 100% CH2Cl2 in hexane

실험 절차

This compound was obtained in 66% yield using the procedure described for the synthesis of N-tert-Butyl-(1-methyl)cyclopropylsulfonamide except 1.2 equivalents of methyl benzoate was used as the electrophile. The compound was purified by column chromatography over SiO2 using 30% to 100% CH2Cl2 in hexane: 1H NMR (CDCl3) δ 1.31 (s, 9H), 1.52 (m, 2H), 1.81 (m, 2H), 4.16 (bs, 1H), 7.46 (m, 2H), 7.57 (m, 1H), 8.05 (d, J=8.5 Hz, 2H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741281B2uspto-grants-2010_06