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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Peroxide → 2-(1-Hydroxycyclopentyl)acetic acid

HRID 1586907
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HRID 1586907 반응식
[C@H:1]12[CH2:7][CH:4](CC1)[CH2:3][C:2]2=[O:8].[C:9]([O-:12])(=[O:11])[CH3:10].[Na+].OO>C(O)(=O)C>[OH:8][C:2]1([CH2:10][C:9]([OH:12])=[O:11])[CH2:3][CH2:4][CH2:7][CH2:1]1
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참가 물질

5

반응물 3

HCID 784Hydrogen PeroxideHCID 517045Sodium AcetateHCID 54006847(1R)-Bicyclo(2.2.1)heptan-2-one

생성물 1

HCID 3482662-(1-Hydroxycyclopentyl)acetic acid수율 67%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

This product is oxidized by the Baeyer-Villiger procedure. (1R)-Norbornanone (81, 18 mmol) is stirred with sodium acetate (9 g, water-free), hydrogen peroxide (27 ml, 30%), and acetic acid (9 ml) at 5° C. in the dark for 40 hours. The reaction is quenched by the addition of sodium sulfite (50 ml of a 10% aqueous solution) at 0° C. The product is extracted twice with EtOAc (600 ml). The extract is washed with the sodium sulfite solution, then with sodium bicarbonate solution (50 ml, saturated), then with sodium chloride solution (saturated), dried and evaporated. The product is chromatographed on silica (380 g, ether) to yield the lacton of 3 hydroxycyclopentane-1-acetic acid (82, 12 mmol, 67%).

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후처리

  1. customThe reaction is quenched by the addition of sodium sulfite (50 ml of a 10% aqueous solution) at 0° C
  2. extractionThe product is extracted twice with EtOAc (600 ml)
  3. washThe extract is washed with the sodium sulfite solution
  4. dry with materialwith sodium bicarbonate solution (50 ml, saturated), then with sodium chloride solution (saturated), dried
  5. customevaporated
  6. customThe product is chromatographed on silica (380 g, ether)

출처 및 근거

ORD 기록
ord-7c2649edde5f475783fa29eb77f4d231
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05216141

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