Hydrochloric Acid → HCID 20163296, 화합물

HRID 246895노트

반응식

HRID 246895 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][C:8]1([C:16](=[O:19])[CH2:17][CH3:18])[CH:13]([CH3:14])[CH2:12][C:11]([CH3:15])=[CH:10][CH2:9]1.[H][H].Cl>C(OCC)C.O>[CH3:7][C:8]1([CH:16]([OH:19])[CH2:17][CH3:18])[CH:13]([CH3:14])[CH2:12][C:11]([CH3:15])=[CH:10][CH2:9]1

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 20163298HCID 20163298, 화합물HCID 21226445Aluminium lithium hydrideHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 20163296HCID 20163296, 화합물

시약·촉매·용매 2

HCID 962Water용매HCID 3283Diethyl Ether용매

실험 절차

A solution of 0.075 moles (2.85 g) lithium aluminum hydride in 150 ml absolute diethyl ether was put in a 250-ml 3-necked flask with a magnetic stirrer, high-power condenser, dropping funnel and internal thermometer. 0.2 moles (36 g) 1-(1,4,6-trimethylcyclohex-3-en-1-yl)propan-1-one (as per Example 4) was added dropwise to this solution with cooling. Then heating with refluxing was carried out for an hour, followed by cooling, and water was added to the reaction mixture until hydrogen evolution ended. Then enough 2N hydrochloric acid was added so that the precipitate formed could be dissolved. Lastly the phases were separated, the organic phase dried with sodium sulfate and the solvent drawn off. After fractional distillation via a 30-cm Vigreux column the desired end product was obtained in practically quantitative yield.

후처리

  1. temperaturewith cooling
  2. temperatureThen heating
  3. temperaturewith refluxing
  4. waitwas carried out for an hour
  5. temperatureby cooling
  6. customformed could
  7. dissolutionbe dissolved
  8. customLastly the phases were separated
  9. dry with materialthe organic phase dried with sodium sulfate
  10. distillationAfter fractional distillation via a 30-cm Vigreux column the desired end product
  11. customwas obtained in practically quantitative yield

출처 및 근거

ORD 기록
ord-23421fa86b8b46e2857c001b7d8da4ea
출처 데이터셋
uspto-grants-1987_11
특허 번호
US04704477

반응 노트

불러오는 중…