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Iodoethane → N,2-Diethyl-N-(4-methyl-1,3-oxazol-2-yl)butanamide

HRID 1112384
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HRID 1112384 반응식
[H-].[Na+].[CH2:3]([CH:5]([CH2:15][CH3:16])[C:6]([NH:8][C:9]1[O:10][CH:11]=[C:12]([CH3:14])[N:13]=1)=[O:7])[CH3:4].[CH2:17](I)[CH3:18]>CN(C)C=O>[CH2:17]([N:8]([C:9]1[O:10][CH:11]=[C:12]([CH3:14])[N:13]=1)[C:6](=[O:7])[CH:5]([CH2:3][CH3:4])[CH2:15][CH3:16])[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 24758Sodium hydrideHCID 12556852HCID 12556852, 화합물

생성물 1

HCID 21323622N,2-Diethyl-N-(4-methyl-1,3-oxazol-2-yl)butanamide수율 51.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Sodium hydride (2.8 g. of a 50% dispersion in oil, 0.058 mol) was added in small portions to a stirred solution of 2-(2-ethylbutyramido)-4-methyloxazole (8.0 g., 0.041 mol) in dimethylformamide (100 ml.) at -5° to 0° C. The mixture was stirred for 2 hours at room temperature and then ethyl iodide (4.7 ml. 0.058 mol) was added. The mixture was stirred for a further 2 hours at room temperature and then poured onto ice-water (250 ml.) and extracted with ether (3 × 100 ml.). The extract was washed with dilute hydrochloric acid, then with sodium chloride solution, dried over sodium sulphate and evaporated. The residue was distilled under vacuum to give the product 4.7 g. (51%) b.p. 71°-72° C/0.3 mm.

후처리

  1. stirringThe mixture was stirred for a further 2 hours at room temperature
  2. additionpoured onto ice-water (250 ml.)
  3. extractionextracted with ether (3 × 100 ml.)
  4. washThe extract was washed with dilute hydrochloric acid
  5. dry with materialwith sodium chloride solution, dried over sodium sulphate
  6. customevaporated
  7. distillationThe residue was distilled under vacuum

출처 및 근거

ORD 기록
ord-bfc49f3e8c504503b63f6545d7828fb9
출처 데이터셋
uspto-grants-1978_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04122183

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