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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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delta-Gluconolactone → (3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-(benzyloxymethyl)-2-(4-chloro-3-((triisopropylsilyloxy)methyl)phenyl)-tetrahydro-2H-pyran-2-ol

HRID 46186
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HRID 46186 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]([Cl:20])=[C:6]([CH:19]=1)[CH2:7][O:8][Si:9]([CH:16]([CH3:18])[CH3:17])([CH:13]([CH3:15])[CH3:14])[CH:10]([CH3:12])[CH3:11].[CH2:21]([Li])[CH2:22][CH2:23][CH3:24].[CH2:26]([OH:37])[C@H:27]1[O:33][C:31](=[O:32])[C@H:30]([OH:34])[C@@H:29]([OH:35])[C@@H:28]1[OH:36]>O1CCCC1>[CH2:21]([O:34][C@@H:30]1[C@@H:29]([O:35][CH2:21][C:22]2[CH:11]=[CH:10][CH:12]=[CH:24][CH:23]=2)[C@H:28]([O:36][CH2:21][C:22]2[CH:14]=[CH:13][CH:15]=[CH:24][CH:23]=2)[C@@H:27]([CH2:26][O:37][CH2:7][C:6]2[CH:5]=[CH:4][CH:3]=[CH:2][CH:19]=2)[O:33][C:31]1([C:2]1[CH:3]=[CH:4][C:5]([Cl:20])=[C:6]([CH2:7][O:8][Si:9]([CH:16]([CH3:18])[CH3:17])([CH:13]([CH3:15])[CH3:14])[CH:10]([CH3:12])[CH3:11])[CH:19]=1)[OH:32])[C:22]1[CH:18]=[CH:16][CH:17]=[CH:24][CH:23]=1
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참가 물질

5

반응물 3

HCID 7027delta-Gluconolactone2회HCID 67153939(5-Bromo-2-chlorobenzyloxy)triisopropylsilane2회HCID 178418339Butyllithium

생성물 1

HCID 67287055(3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-(benzyloxymethyl)-2-(4-chloro-3-((triisopropylsilyloxy)methyl)phenyl)-tetrahydro-2H-pyran-2-ol

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

To a solution of (5-Bromo-2-chlorobenzyloxy)triisopropylsilane (compound 4, 97 g, 257 mmol) from Step 3 in tetrahydrofuran (1 L) at −78° C. under an atmosphere of nitrogen was added dropwise n-butyllithium (2.5 M in hexanes, 103 mL, 257 mmol), and the mixture was stirred for 1.5 h at the same temperature. Then a solution of 2,3,4,6-tetra-O-benzyl-D-glucopyranone (compound 2, 106 g, 198 mmol) from Step 1 in tetrahydrofuran (500 mL) was added dropwise, and the mixture was stirred for 3 h at the same temperature. The reaction mixture was quenched by addition of saturated ammonium chloride solution. After complete addition, the solution was gradually raised to room temperature. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo to yield the title compound as a yellow oil which was used without further purification.

후처리

  1. stirringthe mixture was stirred for 3 h at the same temperature
  2. customThe reaction mixture was quenched by addition of saturated ammonium chloride solution
  3. additionAfter complete addition
  4. customThe organic layer was separated
  5. extractionthe aqueous layer was extracted with ethyl acetate
  6. washThe combined organic layers were washed with brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-a780a61119ba441c9529ed88dfc75f77
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541380B2

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