반응 #309503

ord-f6afb962931c467dae98014409aff6e4

반응 방정식

CS(=O)(=O)OC1CN(C(c2ccccc2)c2ccccc2)C1
1-(diphenylmethyl)azetidin-3-yl methanesulfonate
O=C(Cl)OCCCl
chloroethylchloroformate
CS(=O)(=O)OC1CNC1.Cl
title compound
CS(=O)(=O)OC1CNC1.Cl
Azetidin-3-yl methanesulfonate hydrochloride

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도under reflux for 2.5 hours
  3. 3
    농축The reaction mixture was then concentrated in vacuo
  4. 4
    workup.DISSOLUTIONthe residue was re-dissolved in methanol (100 mL)
  5. 5
    온도heated
  6. 6
    온도under reflux for a further 2.5 hours
  7. 7
    농축concentrated in vacuo

실험 절차

A mixture of 1-(diphenylmethyl)azetidin-3-yl methanesulfonate (WO 97/25322, p 64), (20 g, 63 mmol) and chloroethylchloroformate (10 mL, 95 mmol) in dichloromethane (100 mL) was heated under reflux for 2.5 hours. The reaction mixture was then concentrated in vacuo and the residue was re-dissolved in methanol (100 mL) and heated under reflux for a further 2.5 hours. The mixture was then cooled to room temperature and concentrated in vacuo to afford the title compound as a white solid in quantitative yield, 9.6 g. 1H NMR (400 MHz, DMSO-d6) δ: 3.28 (s, 3H), 4.06 (m, 2H), 4.31 (m, 2H), 5.34 (m, 1H)

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08207198B2uspto-grants-2012_06