Potassium Bromide → tert-Butyl 3,5-dideoxy-2,4-O-(1-methylethylidene)-L-erythro-hexuronate

HRID 877954노트

반응식

HRID 877954 반응식
C1C2CC3N([O])C(C2)CC1C3.[Br-].[K+].[OH:14][CH2:15][C@H:16]1[O:21][C:20]([CH3:23])([CH3:22])[O:19][C@@H:18]([CH2:24][C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[CH2:17]1.Cl[O-].[Na+]>C(Cl)Cl>[CH:15]([C@H:16]1[O:21][C:20]([CH3:23])([CH3:22])[O:19][C@@H:18]([CH2:24][C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[CH2:17]1)=[O:14]

참가 물질

6

실험 절차

To the −15° C. to −5° C. pre-cooled reaction mixture of AZADO (0.002 g), potassium bromide (0.22 g) and methylene chloride (30 ml) added 5 g of tert-butyl 2-((4R,6S)-6-(hydroxymethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate. Stirred the reaction mixture for 15 minutes at −15° C. to −5° C. 19 ml of sodium hypochlorite solution was added to the reaction mixture at same temperature. Stirred the reaction mixture for 15 minutes. Quenched the reaction mixture with 10% aqueous sodium thiosulfate solution. 20 ml of water was added and separated the both aqueous and organic layers. Washed the organic layer with water followed by brine solution. Distilled off the solvent completely to get the title compound as a solid.

후처리

  1. temperatureTo the −15° C. to −5° C. pre-cooled
  2. stirringStirred the reaction mixture for 15 minutes
  3. customQuenched the reaction mixture with 10% aqueous sodium thiosulfate solution
  4. addition20 ml of water was added
  5. customseparated the both aqueous and organic layers
  6. washWashed the organic layer with water
  7. distillationDistilled off the solvent completely

출처 및 근거

ORD 기록
ord-38cfc2d0ed21467189403a902cbdd5ae
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08987444B2

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