반응 #56742

ord-cfb4730cf9e0406fa149a7a8d266f8fc

반응 방정식

C=CCc1c([N+](=O)[O-])ccc2c1O[C@@H](COS(=O)(=O)c1ccc(C)cc1)CO2
toluene-4-sulfonic acid (2R)-8-allyl-7-nitro-2,3-dihydro-benzo(1,4)dioxin-2-ylmethyl ester
O=[O+][O-]
ozone
O=O
oxygen
CCN(C(C)C)C(C)C
diisopropylethylamine
Cc1ccc(S(=O)(=O)OCC2COc3ccc([N+](=O)[O-])c(CC=O)c3O2)cc1
title compound
Cc1ccc(S(=O)(=O)OCC2COc3ccc([N+](=O)[O-])c(CC=O)c3O2)cc1
[7-Nitro-8-(2-oxoethyl)-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONadded
  2. 2
    기타to come to room temperature
  3. 3
    세척It was then washed with 300 mL portions of 2 N HCl (aq), water and saturated brine
  4. 4
    건조dried over magnesium sulfate
  5. 5
    여과filtered
  6. 6
    농축concentrated in vacuum

실험 절차

A solution of 4.2 g (10 mmole) of toluene-4-sulfonic acid (2R)-8-allyl-7-nitro-2,3-dihydro-benzo(1,4)dioxin-2-ylmethyl ester in 400 mL of methylene chloride was cooled in a dry ice/isopropanol bath and saturated with ozone. It was then purged with oxygen and 2.6 g (20 mmole) of diisopropylethylamine added. The mixture was allowed to come to room temperature and stirred under nitrogen for 24 hours. It was then washed with 300 mL portions of 2 N HCl (aq), water and saturated brine, dried over magnesium sulfate, filtered and concentrated in vacuum to give 3.8 g of the (R)-enantiomer of the title compound as a white solid one-quarter hydrate, m.p. 116-120° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07419986B2uspto-grants-2008_09