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Perchloric Acid → (2R,3R)-1,4-bis(phenylmethoxy)butane-2,3-diol

HRID 1029983
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HRID 1029983 반응식
[CH2:1]([O:8][CH2:9][CH:10]1[O:21][CH:11]1[CH2:12][O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl(O)(=O)(=O)=[O:23]>O1CCCC1.O>[CH2:14]([O:13][CH2:12][CH:11]([OH:23])[CH:10]([OH:21])[CH2:9][O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1
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참가 물질

5

반응물 2

HCID 24247Perchloric AcidHCID 13255030(2R,3R)-2,3-Bis((benzyloxy)methyl)oxirane

생성물 1

HCID 3707635(2R,3R)-1,4-bis(phenylmethoxy)butane-2,3-diol

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

4.2 g of the 1,4-bis(benzyloxy)-2,3-epoxybutane thus obtained was dissolved in a mixture comprising 120 ml of tetrahydrofuran and 30 ml of water. Then 30 ml of an aqueous solution containing 6 ml of 60% perchloric acid was added dropwise thereto under ice-cooling and stirring. After stirring at the same temperature for additional 4 hours, the reaction mixture was poured into ice/water and extracted with ether. The extract was washed with water and dried. After distilling off the solvent, the obtained oily residue was purified by column chromatography (silica gel, hexane/ethyl acetate) to thereby give 2.7 g of 1,4-bis(benzyloxy)-2,3-butanediol as a colorless liquid.

후처리

  1. additionwas added dropwise
  2. temperatureunder ice-cooling
  3. stirringAfter stirring at the same temperature for additional 4 hours
  4. extractionextracted with ether
  5. washThe extract was washed with water
  6. customdried
  7. distillationAfter distilling off the solvent
  8. customthe obtained oily residue was purified by column chromatography (silica gel, hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-4d74d5c5dc424b47b4f1e821508320fa
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05102895

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