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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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10-Oxa-tricyclo[5.2.1.0*2,6*]dec-8-ene-3,5-dione → 10-Oxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dione

HRID 407833
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인쇄 미리보기

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HRID 407833 반응식
[CH:1]12[O:10][CH:7]([CH:8]=[CH:9]1)[CH:6]1[CH:2]2[C:3](=[O:12])[CH2:4][C:5]1=[O:11]>CO.[Pd]>[CH:7]12[O:10][CH:1]([CH2:9][CH2:8]1)[CH:2]1[CH:6]2[C:5](=[O:11])[CH2:4][C:3]1=[O:12]
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참가 물질

4

반응물 1

HCID 2067932010-Oxa-tricyclo[5.2.1.0*2,6*]dec-8-ene-3,5-dione

생성물 1

HCID 5935195110-Oxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dione

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

(1RS,2SR,6RS,7SR)-10-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione (2.1 g, 12.8 mmol), prepared in Step 1, is dissolved in warm methanol (180 ml) and the mixture is allowed to cool to room temperature. The mixture is then hydrogenated in the presence of 5% palladium on carbon (approx. 50 mg) at 3.5 bar for 4 hours. The catalyst is removed by filtration through diatomaceous earth and the filtrate is concentrated under reduced pressure to afford (1RS,2SR,6RS,7SR)-10-oxatricyclo[5.2.1.02,6]decane-3,5-dione.

후처리

  1. customThe catalyst is removed by filtration through diatomaceous earth
  2. concentrationthe filtrate is concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-b19fca208a244cc8aad75bf6831d01e5
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08754242B2

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