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Pyrrolidine → 3-(1-Pyrrolidinyl)-9-azabicyclo[3,3,1]non-2-ene-9-carboxylic acid ethylester

HRID 1277378
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HRID 1277378 반응식
[CH2:1]([O:3][C:4]([N:6]1[CH:11]2[CH2:12][CH2:13][CH2:14][CH:7]1[CH2:8][C:9](=O)[CH2:10]2)=[O:5])[CH3:2].[NH:16]1[CH2:20][CH2:19][CH2:18][CH2:17]1>[Ti](Cl)(Cl)(Cl)Cl>[CH2:1]([O:3][C:4]([N:6]1[CH:11]2[CH2:12][CH2:13][CH2:14][CH:7]1[CH:8]=[C:9]([N:16]1[CH2:20][CH2:19][CH2:18][CH2:17]1)[CH2:10]2)=[O:5])[CH3:2]
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참가 물질

4

반응물 2

HCID 31268PyrrolidineHCID 54360990Ethyl 3-oxo-9-azabicyclo[3.3.1]nonane-9-carboxylate

생성물 1

HCID 538825703-(1-Pyrrolidinyl)-9-azabicyclo[3,3,1]non-2-ene-9-carboxylic acid ethylester

시약·촉매·용매 1

HCID 24193Titanium Tetrachloride촉매

실험 절차

At room temperature, under a nitrogen atmosphere and with stirring, a solution of 110 g of titanium tetrachloride in 450 ml of petroleum ether is added dropwise, within 2.5 hours, to a solution of 223 g of 9-azabicyclo-[3,3,1]nonan-3-one-9-carboxylic acid ethyl ester (e) and 300 g of pyrrolidine in 2.5 liters of absolute petroleum ether (b.p. 50° to 70° C.). The mixture is stirred for 24 hours. The light-yellow precipitate formed is filtered, suspended in benzene, suctionfiltered and washed with benzene. The united filtrates are concentrated in a vacuum; the orange-red oil which remains behind is purified through vacuum distillation to obtain 260 g (93.5 percent) of yellow, viscous oil (b.p. 140° C. at 6.7 Pa.)

후처리

  1. stirringThe mixture is stirred for 24 hours
  2. customThe light-yellow precipitate formed
  3. filtrationis filtered
  4. washwashed with benzene
  5. concentrationThe united filtrates are concentrated in a vacuum
  6. distillationthe orange-red oil which remains behind is purified through vacuum distillation
  7. customto obtain 260 g (93.5 percent) of yellow, viscous oil (b.p. 140° C. at 6.7 Pa.)

출처 및 근거

ORD 기록
ord-141b6bfc8f5b48429eeec9999cd8a81a
출처 데이터셋
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04277472

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