홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

2,6,10-Trimethyl-dodeca-4,8-dien-1-al → 2,6,10-Trimethyl-dodecan-1-al

HRID 1414463
노트
인쇄 미리보기

반응식

HRID 1414463 반응식
[CH3:1][CH:2]([CH2:5][CH:6]=[CH:7][CH:8]([CH3:16])[CH2:9][CH:10]=[CH:11][CH:12]([CH3:15])[CH2:13][CH3:14])[CH:3]=[O:4]>O1CCCC1.[Pd]>[CH3:1][CH:2]([CH2:5][CH2:6][CH2:7][CH:8]([CH3:16])[CH2:9][CH2:10][CH2:11][CH:12]([CH3:15])[CH2:13][CH3:14])[CH:3]=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 543547842,6,10-Trimethyl-dodeca-4,8-dien-1-al

생성물 1

HCID 189566932,6,10-Trimethyl-dodecan-1-al수율 92.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

22 g (0.1 mole) of 2,6,10-trimethyl-dodeca-4,8-dien-1-al are dissolved in 20 ml of tetrahydrofuran, 1 g of a palladium/charcoal catalyst (1%) is added and hydrogenation is carried out at 70° C until the absorption of hydrogen has ceased. The catalyst is then filtered off, the solvent distilled off and the residue is fractionated through a descending condenser. 21 g of 2,6,10-trimethyl-dodecan-1-al are obtained (yield, 93% of theory). B.p. = 80° - 81° C at 0.3 mm Hg; nD25 = 1.4456. Odor: bitter, greener and more aldehyde-like orange scent.

후처리

  1. customhydrogenation is carried out at 70° C until the absorption of hydrogen
  2. filtrationThe catalyst is then filtered off
  3. distillationthe solvent distilled off
  4. customthe residue is fractionated through a descending condenser

출처 및 근거

ORD 기록
ord-488f29d7f5754b8fab0ceaf172aea2f3
출처 데이터셋
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04001336

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트