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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylsilane → 2,3-Dihydro-4,7-dimethoxy-1H-indene

HRID 389295
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HRID 389295 반응식
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]2[C:4]=1[CH2:5][CH2:6][C:7]2=O.C([SiH](CC)CC)C>FC(F)(F)C(O)=O>[CH3:13][O:12][C:9]1[CH:10]=[CH:11][C:3]([O:2][CH3:1])=[C:4]2[C:8]=1[CH2:7][CH2:6][CH2:5]2
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참가 물질

4

반응물 2

HCID 12052TriethylsilaneHCID 6060124,7-dimethoxy-2,3-dihydro-1H-inden-1-one

생성물 1

HCID 126541332,3-Dihydro-4,7-dimethoxy-1H-indene

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

To the cooled and stirred suspension of 4,7-Dimethoxyindan-1-one (35 gm, 0.182 mole) in Triethyl silane (105.7 gm, 0.909 mole), added Trifluoroacetic acid (350 ml) at 10-15° C. The stirring was continued at room temperature for 2 hours and quenched into the water. It was extracted with Ethyl acetate. The Ethyl acetate layer was washed with Sodium bicarbonate solution, dried over Sodium sulphate and evaporated to give crude mass which was purified by column chouromatography using 5% Ethyl acetate in hexane (22.5 gm).

후처리

  1. temperatureTo the cooled
  2. customquenched into the water
  3. extractionIt was extracted with Ethyl acetate
  4. washThe Ethyl acetate layer was washed with Sodium bicarbonate solution
  5. dry with materialdried over Sodium sulphate
  6. customevaporated
  7. customto give crude mass which
  8. customwas purified by column chouromatography

출처 및 근거

ORD 기록
ord-b02e0f252d6443fe8f380246ef849ad5
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08378118B2

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