반응 #2146743

ord-9401873432664ee79db02dfe3d817f3c

반응 방정식

COC1O[C@H](COCc2ccc(Cl)cc2Cl)[C@H](OCc2ccc(Cl)cc2Cl)[C@H]1CC(=O)[O-]
(3R,4R,5R)-5-(2,4-dichloro-benzyloxymethyl)-4-(2,4-dichlorobenzyloxy)-2-methoxy-tetrahydrofuran-3-acetate
C[O-].[Na+]
NaOMe
COC1O[C@H](COCc2ccc(Cl)cc2Cl)[C@@H](OCc2ccc(Cl)cc2Cl)[C@H]1O
(3R,4S,5R)-5-(2,4-Dichlorobenzyloxymethyl)-4-(2,4-dichlorobenzyloxy)-2-methoxy-tetrahydrofuran-3-ol

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The reaction mixture is concentrated
  2. 2
    workup.DISSOLUTIONdissolved in ethyl acetate (180 ml)
  3. 3
    세척washed with 1 N HCl solution and saturated brine
  4. 4
    건조dried (anhyd Na2SO4)
  5. 5
    농축concentrated

실험 절차

To a solution of (3R,4R,5R)-5-(2,4-dichloro-benzyloxymethyl)-4-(2,4-dichlorobenzyloxy)-2-methoxy-tetrahydrofuran-3-acetate I-1 (10 g, 19.1 mmol) in MeOH (150 ml) is added a solution of 30% NaOMe in MeOH (5.37 ml, 28.6 mmol, 1.5 equiv.) and the reaction is stirred at room temperature for 30 mins. The reaction mixture is concentrated and dissolved in ethyl acetate (180 ml), washed with 1 N HCl solution and saturated brine, dried (anhyd Na2SO4) and concentrated to give (3R,4S,5R)-5-(2,4-Dichlorobenzyloxymethyl)-4-(2,4-dichlorobenzyloxy)-2-methoxy-tetrahydrofuran-3-ol I-2 as yellowish oil. The obtained crude compound is used for the next step without further purification.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08278282B2uspto-grants-2012_10