Benzaldehyde → 1-Cyclohexyl-4-dimethylamino-2-phenyl-2-buten-1-ol

HRID 845144

反応式

HRID 845144 の反応式
C([Li])CCC.C(C1C=C(C(C)C)C=C(C(C)C)C=1S(NN=[C:26]([C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[CH2:27][CH2:28][N:29]([CH3:31])[CH3:30])(=O)=O)(C)C.[CH:38](=[O:45])[C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1.Cl>CCCCCC.COCCOC.C(OCC)C>[CH:39]1([CH:38]([OH:45])[C:26]([C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=2)=[CH:27][CH2:28][N:29]([CH3:30])[CH3:31])[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40]1

参加物

8

反応物 4

HCID 240BenzaldehydeHCID 313Hydrochloric AcidHCID 86741729beta-Dimethylaminopropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazoneHCID 178418339Butyllithium

生成物 1

HCID 538458471-Cyclohexyl-4-dimethylamino-2-phenyl-2-buten-1-ol

試薬・触媒・溶媒 3

HCID 3283Diethyl Ether溶媒HCID 8058Hexane溶媒HCID 80711,2-Dimethoxyethane溶媒

反応条件

温度
0 °C

実験手順

A 1.5M solution (29 cc) of n-butyllithium in hexane is added to a solution of β-dimethylaminopropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazone (9.15 g) in 1,2-dimethoxyethane (100 cc) kept under a nitrogen atmosphere at a temperature in the region of -75° C. The orange solution obtained is then stirred for 15 minutes at a temperature in the region of 0° C., and then cooled to a temperature in the region of -40° C. Benzaldehyde (2.2 cc) is then added, and then the reaction mixture is stirred for 1 hour at a temperature in the region of 20° C. A 1N aqueous solution (100 cc) of hydrochloric acid is then added with stirring, followed by ethyl ether (100 cc). The aqueous phase is separated; the organic phase is extracted with a 0.1N aqueous solution (25 cc) of hydrochloric acid. The aqueous phases are combined, washed with ether (2×50 cc) and then made alkaline to a pH in the region of 10 with sodium hydroxide solution, and then extracted with ethyl acetate (3×50 cc). The organic phases are combined, dried over magnesium sulphate, filtered and then concentrated to dryness under reduced pressure (2.7 kPa) at 40° C. In this way 4-dimethylamino-1,2-diphenyl-2-buten-1-ol (Z) (5.2 g) is obtained in the form of white crystals melting at 75° C.

後処理

  1. customkept under a nitrogen atmosphere at a temperature in the region of -75° C
  2. customThe orange solution obtained
  3. temperaturecooled to a temperature in the region of -40° C
  4. stirringthe reaction mixture is stirred for 1 hour at a temperature in the region of 20° C
  5. stirringwith stirring
  6. customThe aqueous phase is separated
  7. extractionthe organic phase is extracted with a 0.1N aqueous solution (25 cc) of hydrochloric acid
  8. washwashed with ether (2×50 cc)
  9. extractionextracted with ethyl acetate (3×50 cc)
  10. dry with materialdried over magnesium sulphate
  11. filtrationfiltered
  12. concentrationconcentrated to dryness under reduced pressure (2.7 kPa) at 40° C

出典と根拠

ORDレコード
ord-8a9fe2ab480a48ca8f327a0ec6304946
出典データセット
uspto-grants-1988_07
特許番号
US04755599

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