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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 917388생성일: 2026년 10월 26일

Ethyl 2-chloroacetoacetate → Ethyl 2-anilino-4-methyl-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/917388

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 2-chloroacetoacetateHCID 11858—
반응물PhenylthioureaHCID 676454—
용매EthanolHCID 702—
생성물Ethyl 2-anilino-4-methyl-1,3-thiazole-5-carboxylateHCID 80777291.5%

반응 단계

To 70 ml of ethanol, 10.7 g (70 mmol) of phenylthiourea and 11.6 g (70 mmol) of ethyl 2-chloro-3-oxobutanate were dissolved, followed by heating under refluxing for 8 hours. The reaction liquid was concentrated and dissolved in ethyl acetate and the organic layer was washed with an aqueous solution of sodium carbonate, water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentrating under reduced pressure. Solid obtained was washed with diisopropyl ether to obtain 16.8 g (yield: 91%) of ethyl 4-methyl-2-(N-phenylamino)thiazole-5-carboxylate. (2) To 50 ml of ethanol, 12.8 g (49 mmol) of ethyl-4-methyl-2-(N-phenylamino)thiazole-5-carboxylate was dissolved, followed by adding 24 g (150 mmol) of 25% sodium hydroxide aqueous solution, and stirring at 80° C. for 15 hours. The reaction liquid was poured into ice water, and acetic acid was added to make acidic. Crystal precipitated was filtered, washed with water and a mixed solvent of hexane/ethyl acetate and dried to obtain 5.50 g (yield: 48%) of 4-methyl-2-(N-phenylamino)thiazole-5-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07273878B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-6f9ad1ae7dd8467e9631e333a8a5a164
출처 메모uspto-grants-2007_09