Diethylamine → 1-(2,2-Diethoxyethyl)cyclohexane-1-carbonitrile

HRID 462511

반응식

HRID 462511 반응식
C(NCC)C.C([Li])CCC.[CH:11]1([C:17]#[N:18])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1.[CH2:19]([O:21][CH:22]([O:25][CH2:26][CH3:27])[CH2:23]Br)[CH3:20]>CCCCCC>[CH2:19]([O:21][CH:22]([O:25][CH2:26][CH3:27])[CH2:23][C:11]1([C:17]#[N:18])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1)[CH3:20]

참가 물질

6

반응물 4

HCID 8021DiethylamineHCID 69834CyanocyclohexaneHCID 74852Ethane, 2-bromo-1,1-diethoxy-HCID 178418339Butyllithium

생성물 1

HCID 132173501-(2,2-Diethoxyethyl)cyclohexane-1-carbonitrile

시약·촉매·용매 1

HCID 8058Hexane용매

반응 조건

온도
-70 °C

실험 절차

51.7 ml (0.5 mol) of anhydrous diethylamine are added dropwise to 312.5 ml (0.5 mol) of a 15% solution of n-butyl-lithium in hexane at -10° C. under an inert gas blanket. The batch is stirred for 10 minutes and then cooled to -70° C. Within 30 minutes, 54.6 g of cyclohexane-carbonitrile are added dropwise, after a further 30 minutes 98.5 g of bromoacetaldehyde-diethylacetal are added within 1 hour, and the batch is maintained for 24 hours at low temperature. Subsequently, it is warmed to room temperature, given onto 100 g of ice, extracted twice with 500 ml of ethyl acetate, the organic phase is dried over sodium sulfate, concentrated in vacuo, and the residue is subjected to vacuum distillation.

후처리

  1. waitWithin 30 minutes
  2. additionare added within 1 hour
  3. temperaturethe batch is maintained for 24 hours at low temperature
  4. temperatureSubsequently, it is warmed to room temperature
  5. extractionextracted twice with 500 ml of ethyl acetate
  6. dry with materialthe organic phase is dried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. distillationthe residue is subjected to vacuum distillation

출처 및 근거

ORD 기록
ord-26fc452980d64f33bffc69f7d14a2f3a
출처 데이터셋
uspto-grants-1985_05
특허 번호
US04515960

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