Diethyl Ether → Ethyl 2-(2-phenyl-1,3-thiazol-4-yl)acetate

HRID 258576

반응식

HRID 258576 반응식
Br[CH2:2][C:3](=O)[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6].[C:11]([NH2:19])(=[S:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.CCOCC>C(O)C>[C:12]1([C:11]2[S:18][CH:2]=[C:3]([CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6])[N:19]=2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 575284Ethyl 4-bromo-3-oxobutanoateHCID 683563Thiobenzamide

생성물 1

HCID 2797666Ethyl 2-(2-phenyl-1,3-thiazol-4-yl)acetate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl γ-bromoacetoacetate [2.62 g, 0.9-1.0 mole, described by A. Burger and G. E. Ullyot, J. Org. Chem., 12, 346 (1947)]is added in one portion to a suspension of thiobenzamide [117.5 g, 0.857 mole, described by A. Silberg et al., Ber., 94, 2887 (1961)] in ethanol. The clear solution is refluxed on a steam bath for 2 hr, cooled and slowly added with stirring to ether (3500 ml). The white crystalline precipitate is collected, washed with ether and partitioned between water and ether. Sodium bicarbonate is added in portions until the mixture is alkaline. The mixture is extracted with ether, the ether solution is washed with saturated sodium chloride solution, dried, and evaporated to give ethyl 2-phenylthiazole-4-acetate (VII; R1 = H, R9 = CH2CH3), γmaxCHCl3 1725 cm-1.

후처리

  1. temperatureThe clear solution is refluxed on a steam bath for 2 hr
  2. temperaturecooled
  3. additionslowly added
  4. customThe white crystalline precipitate is collected
  5. washwashed with ether
  6. custompartitioned between water and ether
  7. additionSodium bicarbonate is added in portions until the mixture
  8. extractionThe mixture is extracted with ether
  9. washthe ether solution is washed with saturated sodium chloride solution
  10. customdried
  11. customevaporated

출처 및 근거

ORD 기록
ord-2964eaeb2c594e1793a3fd1e6a96a762
출처 데이터셋
uspto-grants-1977_07
특허 번호
US04033977

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