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Triethylamine → 2-(2-Phenylpropyl)imidazolidin-4-one

HRID 1948390
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인쇄 미리보기

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HRID 1948390 반응식
[C:1]1([CH:7]([CH3:11])[CH2:8][CH:9]=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[NH2:13][CH2:14][C:15]([NH2:17])=[O:16].C(N(CC)CC)C.C([O-])([O-])=O.[K+].[K+]>C(O)C>[C:1]1([CH:7]([CH3:11])[CH2:8][CH:9]2[NH:17][C:15](=[O:16])[CH2:14][NH:13]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 11430Potassium CarbonateHCID 859793-PhenylbutanalHCID 2723639Glycinamide hydrochloride

생성물 1

HCID 575228982-(2-Phenylpropyl)imidazolidin-4-one

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
60 °C

실험 절차

A mixture of 3-phenylbutanal (Trifernal®, 0.67 g, 4.5 mmol), glycinamide hydrochloride (0.50 g, 4.5 mmol), triethylamine (0.46 g, 4.5 mmol) and K2CO3 in ethanol (4 ml) was heated to 60° C. for 24 h. Then the solvent was removed under vacuum at 40° C. The residue was taken up in ether and the solvent evaporated to yield 0.52 g (57%) of a highly viscous oil as a mixture of diastereoisomers.

후처리

  1. customThen the solvent was removed under vacuum at 40° C
  2. customthe solvent evaporated
  3. customto yield 0.52 g (57%) of a highly viscous oil
  4. additionas a mixture of diastereoisomers

출처 및 근거

ORD 기록
ord-625699e9e27741c5be5c208f1d623f40
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399499B2

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