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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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L-Fucal → 1,5-anhydro-3-oxo-2,3,6-trideoxy-L-threo-hex-1-enitol

HRID 1155326
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HRID 1155326 반응식
[CH3:1][C@@H:2]1[O:7][CH:6]=[CH:5][C@H:4]([OH:8])[C@@H:3]1[OH:9]>C1C=CC=CC=1.C(=O)([O-])[O-].[Ag+2].C([O-])([O-])=O.[Ag+].[Ag+]>[O:8]=[C:4]1[C@H:3]([OH:9])[C@H:2]([CH3:1])[O:7][CH:6]=[CH:5]1
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참가 물질

5

반응물 1

HCID 11083911L-Fucal

생성물 1

HCID 128167791,5-anhydro-3-oxo-2,3,6-trideoxy-L-threo-hex-1-enitol

시약·촉매·용매 3

HCID 92796Silver carbonate촉매HCID 178418647HCID 178418647, 화합물촉매HCID 241Benzene용매

실험 절차

In a 250 milliliter round-bottomed flask, 1 gram of L-fucal [Example 5 product] is dissolved in 100 milliliters of benzene. To this solution was added 20-25 grams of silver carbonate on celite (Fetizon's reagent), prepared as described below, and the mixture was stirred. The flask was equipped for simple distillation, and 20-25 milliliters of solvent was removed by distillation. During this time the yellow Fetizon's reagent becomes dark brown. The distillation assembly is replaced with an efficient reflux condenser and the mixture is refluxed for 1 hour, after which time the reaction is generally completed as judged by t.l.c. monitoring. The hot mixture is filtered through celite and the filtrate evaporated under reduced pressure to give 1,5-anhydro-3-oxo-2,3,6-trideoxy-L-threo-hex-1-enitol.

후처리

  1. customprepared
  2. customwas removed by distillation
  3. distillationThe distillation
  4. customassembly is replaced with an efficient reflux condenser
  5. temperaturethe mixture is refluxed for 1 hour
  6. filtrationThe hot mixture is filtered through celite
  7. customthe filtrate evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-166bebeb578e4543948968928c145247
출처 데이터셋
uspto-grants-1981_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04301276

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