Sodium Hydroxide → 3-(5-Hydroxypentylidene)-7,7-ethylenedioxy-cis-bicyclo[3,3,0]octane

HRID 1654241노트

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HRID 1654241 반응식
[C:1]([CH2:4][CH2:5][CH2:6][CH:7]=[C:8]1[CH2:15][C@@H:14]2[C@@H:10]([CH2:11][C:12]3([O:19][CH2:18][CH2:17][O:16]3)[CH2:13]2)[CH2:9]1)(O)=[O:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+]>O1CCCC1>[OH:2][CH2:1][CH2:4][CH2:5][CH2:6][CH:7]=[C:8]1[CH2:15][C@@H:14]2[C@@H:10]([CH2:11][C:12]3([O:16][CH2:17][CH2:18][O:19]3)[CH2:13]2)[CH2:9]1

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 228526373-(4-Carboxybutylidene)-7,7-ethylenedioxy-cis-bicyclo[3,3,0]octane

생성물 1

HCID 228526963-(5-Hydroxypentylidene)-7,7-ethylenedioxy-cis-bicyclo[3,3,0]octane수율 100.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

49.10 g of 3-(4-carboxybutylidene)-7,7-ethylenedioxy-cis-bicyclo[3,3,0]octane (prepared as described in Preparation 1) in 150 ml of tetrahydrofuran were added dropwise to a suspension of 10.50 g of lithium aluminum hydride in 675 ml of tetrahyarofuran, whilst cooling with ice. The mixture was then heated under reflux for 80 minutes. Upon completion of the reaction, 42 ml of a 4% w/v aqueous solution of sodium hydroxide were added, and the mixture was stirred at room temperature. The resulting precipitate was removed by filtration, and the filtrate was condensed by evaporation under reduced pressure, giving 46.90 g of a residue. On purifying the residue by silica gel column chromatography, 40.10 g of the title compound were obtained as an oil, from the fractions eluted with hexane containing 20-30% by volume of ethyl acetate.

후처리

  1. temperaturewhilst cooling with ice
  2. temperatureThe mixture was then heated
  3. temperatureunder reflux for 80 minutes
  4. additionwere added
  5. customThe resulting precipitate was removed by filtration
  6. customcondensed
  7. customby evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-80b7dee9b4374a499355a78bbdb4027c
출처 데이터셋
uspto-grants-1995_04
특허 번호
US05405870

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