Ammonium Acetate → HCID 54285037, 화합물

HRID 2255237노트

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HRID 2255237 반응식
[C:1]([O:10][CH2:11][C:12]([C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=1)=O)(=O)[CH2:2][CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].C([O-])(=O)C.[NH4+:25]>C(O)(=O)C>[Cl:20][C:17]1[CH:18]=[CH:19][C:14]([C:12]2[N:25]=[C:1]([CH2:2][CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5])[O:10][CH:11]=2)=[CH:15][CH:16]=1

참가 물질

4

반응물 2

HCID 517165Ammonium AcetateHCID 539218831-[2-(4-Chlorophenyl)-2-oxoethyl] 4-ethyl butanedioate

생성물 1

HCID 54285037HCID 54285037, 화합물수율 31.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
110 °C

실험 절차

A mixture of 2-(4-chlorophenyl)-2-oxoethyl ethyl succinate (7.6 g), ammonium acetate (9.8 g) and acetic acid (80 ml) was stirred for an hour at 110° C. and refluxed for 2 hours. The solvent was distilled off. The residue was diluted with water, made basic by addition of aqueous sodium hydrogen carbonate solution and then extracted with ethyl acetate. The ethyl acetate layer was washed with water, and dried over MgSO4. After removal of the solvent, the oily residue was subjected to a silica gel column chromatography. Crystals of ethyl 4-(4-chlorophenyl)-2-oxazolepropionate (2.23 g, 31%) were obtained from the fraction eluted with ethyl acetate-hexane (1:3, V/V). Recrystallization from ethyl acetate-hexane gave colorless plate crystals of mp 65°-66° C.

후처리

  1. temperaturerefluxed for 2 hours
  2. distillationThe solvent was distilled off
  3. additionThe residue was diluted with water
  4. additionmade basic by addition of aqueous sodium hydrogen carbonate solution
  5. extractionextracted with ethyl acetate
  6. washThe ethyl acetate layer was washed with water
  7. dry with materialdried over MgSO4
  8. customAfter removal of the solvent

출처 및 근거

ORD 기록
ord-ba655258c8384add8dbf8f5c3d8ff282
출처 데이터셋
uspto-grants-1993_08
특허 번호
US05239080

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