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Benzene → HCID 67716575, 화합물

HRID 234571
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반응식

HRID 234571 반응식
[CH2:1]([C:7]1[CH:19]=[CH:18][C:10]([C:11]([NH:13][CH2:14][C:15]([OH:17])=[O:16])=O)=[CH:9][CH:8]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].C1C=CC=CC=1.ClC(OCC)=O>C(N(CC)CC)C>[CH2:1]([C:7]1[CH:19]=[CH:18][C:10]([CH:11]2[N:13]=[CH:14][C:15](=[O:17])[O:16]2)=[CH:9][CH:8]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 241BenzeneHCID 10928Ethyl chloroformateHCID 3979718HCID 3979718, 화합물

생성물 1

HCID 67716575HCID 67716575, 화합물

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

In a 50 ml-three-necked flask, 1.00 g (3.80 mM) of N-(4-hexylbenzoyl)glycine and 19 ml of dry benzene were placed. To the mixture, 0.53 ml (3.81 mM) of triethylamine was added at room temperature under stirring, followed by addition of 0.37 ml (3.87 mM) of ethyl chloroformate and further stirring for 20 minutes at room temperature to precipitate triethylamine hydrochloride. The resultant hydrochloride was filtered off and the solvent of the filtrate was distilled off. The residue was dried under reduced pressure to obtain 2-(4-hexylphenyl)-5-oxazolone.

후처리

  1. stirringfurther stirring for 20 minutes at room temperature
  2. customto precipitate triethylamine hydrochloride
  3. filtrationThe resultant hydrochloride was filtered off
  4. distillationthe solvent of the filtrate was distilled off
  5. customThe residue was dried under reduced pressure

출처 및 근거

ORD 기록
ord-22fd9e8f74034778aea946c110cd662b
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05595685

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