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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 18703984, 화합물 → HCID 13244670, 화합물

HRID 2288069
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HRID 2288069 반응식
[CH3:1][C:2]1([CH3:16])[CH2:11][C:10]2[C:9](C(O)=O)=[CH:8][CH:7]=[CH:6][C:5]=2[C:4](=[O:15])[CH2:3]1>N1C2C(=CC=CC=2)C=CC=1.CC(=O)OCC.[Cu]>[CH3:1][C:2]1([CH3:16])[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:15])[CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 18703984HCID 18703984, 화합물

생성물 1

HCID 13244670HCID 13244670, 화합물수율 34.4%

시약·촉매·용매 3

HCID 23978Copper촉매HCID 7047Quinoline용매HCID 8857Ethyl Acetate용매

실험 절차

2.2 g (10 mmol) of 7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-1-naphthalenecarboxylic acid were heated to 180° C. for 5 h with 2.2 g of copper powder in 22 g of quinoline. After cooling, the mixture was diluted with EA, and the copper was filtered off and then washed several times with dil. hydrochloric acid. After concentration of the organic phase in a rotary evaporator and purification by chromatography on silica gel using cyclohexane/EA 6:1, 0.6 g of 3,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one was obtained.

후처리

  1. temperatureAfter cooling
  2. filtrationthe copper was filtered off
  3. washwashed several times with dil. hydrochloric acid
  4. customAfter concentration of the organic phase in a rotary evaporator and purification by chromatography on silica gel

출처 및 근거

ORD 기록
ord-4761e5ed8730430aacea6330a26e22ab
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06087399

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