반응 #1453529

ord-aa37bea96fbe49a3bfeece8564a61d37

반응 방정식

OC[C@@H](O)COCc1ccccc1
(2R)-3-(benzyloxy)propane-1,2-diol
ClCCCl
1,2-dichloroethane
[Na+].[OH-]
sodium hydroxide
ClCCCl
1,2-dichloroethane
[Na+].[OH-]
sodium hydroxide
ClCCCl
1,2-dichloroethane
c1ccc(COC[C@H]2COCCO2)cc1
title compound
c1ccc(COC[C@H]2COCCO2)cc1
(2S)-2-[(benzyloxy)methyl]-1,4-dioxane

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITAfter 8 h
  2. 2
    workup.WAITAfter 72 h
  3. 3
    세척washed with water and brine
  4. 4
    건조dried over sodium sulfate
  5. 5
    농축concentrated
  6. 6
    기타The residue was purified by flash column chromatography (silica, ethylacetate/hexanes)

실험 절차

(2R)-3-(benzyloxy)propane-1,2-diol (2.00 g, 11.0 mmol) and tetrabutylammonium bromide (708 mg, 2.20 mmol) were dissolved in 50 mL of 1,2-dichloroethane, then 50 mL of a 50% (w/w) aqueous sodium hydroxide solution was added quickly and the mixture was heated to 50° C. After 18 h, an additional 50 mL of 1,2-dichloroethane and 50 mL of 50% (w/w) sodium hydroxide solution was added. After 8 h, additional 50 mL of 1,2-dichloroethane was added. After 72 h, the mixture was diluted in diethyl ether, washed with water and brine, then dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography (silica, ethylacetate/hexanes) to afford the title compound. 1H NMR (600 MHz, CDCl3) δ 7.26-7.35 (m, 5H); 4.51-4.56 (m, 2H); 3.72-3.82 (m, 4H); 3.67-3.71 (m, 1H); 3.58-3.64 (m, 1H); 3.38-3.48 (m, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07893081B2uspto-grants-2011_02