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Methyl Acrylate → Methyl 2-(4-(4-chlorophenyl)-2-oxo-4-oxazolin-5-yl)propionate

HRID 47924
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HRID 47924 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:9][C:10](=[O:13])[O:11][CH:12]=2)=[CH:4][CH:3]=1.[C:14]([O:18][CH3:19])(=[O:17])[CH:15]=[CH2:16].C(N(CC)CC)C>CO>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[NH:9][C:10](=[O:13])[O:11][C:12]=2[CH:15]([CH3:16])[C:14]([O:18][CH3:19])=[O:17])=[CH:6][CH:7]=1
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참가 물질

5

반응물 3

HCID 7294Methyl AcrylateHCID 8471TriethylamineHCID 114241254-(4-Chlorophenyl)-2,3-dihydro-1,3-oxazol-2-one

생성물 1

HCID 11150230Methyl 2-(4-(4-chlorophenyl)-2-oxo-4-oxazolin-5-yl)propionate수율 65%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
5 °C

실험 절차

4-(4-Chlorophenyl)-2-oxo-4-oxazoline (3.0 g) was dissolved in methanol (30 mL) and methyl acrylate (1.66 mL) and triethylamine (2.14 mL) were added. The obtained mixture was stirred with reflux for 6 h, and the solvent was concentrated under reduced pressure. Isopropanol (9 mL) and isopropyl ether (21 mL) were added, and the mixture was allowed to stand at room temperature overnight and was cooled to not higher than 5° C. and stirred for 1 h. The precipitated crystals were collected by filtration and washed with isopropyl ether to give the title compound (2.81 g; yield 65.0%).

후처리

  1. temperaturewith reflux for 6 h
  2. concentrationthe solvent was concentrated under reduced pressure
  3. additionIsopropanol (9 mL) and isopropyl ether (21 mL) were added
  4. stirringstirred for 1 h
  5. filtrationThe precipitated crystals were collected by filtration
  6. washwashed with isopropyl ether

출처 및 근거

ORD 기록
ord-f8d0ae6f6fd14175b7df246221d57654
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06699995B1

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