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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2,2,4,8-Tetramethyl-1,2-dihydroquinoline → HCID 20543085, 화합물

HRID 616232
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인쇄 미리보기

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HRID 616232 반응식
[CH3:1][C:2]1([CH3:14])[CH:11]=[C:10]([CH3:12])[C:9]2[C:4](=[C:5]([CH3:13])[CH:6]=[CH:7][CH:8]=2)[NH:3]1.[H][H]>[Rh]>[CH3:1][C:2]1([CH3:14])[CH2:11][CH:10]([CH3:12])[CH:9]2[CH:4]([CH:5]([CH3:13])[CH2:6][CH2:7][CH2:8]2)[NH:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 36133852,2,4,8-Tetramethyl-1,2-dihydroquinolineHCID 178418361HCID 178418361, 화합물3회

생성물 1

HCID 20543085HCID 20543085, 화합물

시약·촉매·용매 1

HCID 23948Rhodium촉매

실험 절차

2,2,4,8-tetramethyldecahydroquinoline was prepared by reacting 74 grams of 2,2,4,8-tetramethyl-1,2-dihydroquinoline with hydrogen in the presence of 2 grams of rhodium at 5% by weight on charcoal at a temperature of 200° C., a pressure of 1000 psig, and over a period of 8 hours. The desired product was confirmed by NMR spectral analysis and carbon, hydrogen, nitrogen analysis (calculated content for C13H25N is the same as above and analyzed contents were 80.03% carbon, 13.38% hydrogen, and 6.09% nitrogen). The product was 90% pure as determined by vapor pressure chromotography and boiled at 65° C. at 0.6 mm of Hg.

후처리

  1. customat a temperature of 200° C.

출처 및 근거

ORD 기록
ord-ad124dc24c514d14a0c37c172c612995
출처 데이터셋
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04073770

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