Benzyl Alcohol → Benzyl 2,3,4-tri-O-acetyl-alpha-D-lyxopyranoside

HRID 964863노트

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HRID 964863 반응식
[C:1]([O:4][C@H:5]1[C@@H:10]([O:11][C:12](=[O:14])[CH3:13])[C@H:9]([O:15][C:16](=[O:18])[CH3:17])[CH2:8][O:7][C@@H:6]1Br)(=[O:3])[CH3:2].[CH2:20]([OH:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[Hg]C#N>C(#N)C.[Hg]Br>[C:1]([O:4][C@H:5]1[C@@H:10]([O:11][C:12](=[O:14])[CH3:13])[C@H:9]([O:15][C:16](=[O:18])[CH3:17])[CH2:8][O:7][C@@H:6]1[O:27][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)(=[O:3])[CH3:2]

참가 물질

6

반응물 3

HCID 244Benzyl AlcoholHCID 130488932,3,4-tri-O-acetyl-alpha-lyxopyranosyl bromideHCID 14367217Cyanide mercury

생성물 1

HCID 67638320Benzyl 2,3,4-tri-O-acetyl-alpha-D-lyxopyranoside수율 96.1%

시약·촉매·용매 2

HCID 24830Mercury bromide촉매HCID 6342Acetonitrile용매

실험 절차

A solution of compound 2 (21 g, 61.9 mmol) in acetonitrile (200 ml) and benzyl alcohol (9.6 ml, 92.3 mmol) was vigorously stirred with molecular sieves (4 Å, 25 g), mercury bromide (25 g, 69.4 mmol), mercury cyanide (18.2 g, 12.0 mmol) under argon for 18 hours. The organic layer was filtered through celite and diluted with dichloromethane (250 ml) which was washed with water, aq. NaHCO3 and aq. NaCl and dried (Na2 SO4). The solvent was filtered and then evaporated under reduced pressure. The syrupy residue was chromatographed on silica gel (filter technique) using 1.5:1 hexane-ethyl acetate to give 3 (21.8 g, 90.0%).

후처리

  1. filtrationThe organic layer was filtered through celite
  2. additiondiluted with dichloromethane (250 ml) which
  3. washwas washed with water, aq. NaHCO3 and aq. NaCl
  4. customdried (Na2 SO4)
  5. filtrationThe solvent was filtered
  6. customevaporated under reduced pressure
  7. customThe syrupy residue was chromatographed on silica gel (filter technique)

출처 및 근거

ORD 기록
ord-d563b2c918d148debb74d76c47142d92
출처 데이터셋
uspto-grants-1998_06
특허 번호
US05773239

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