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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243662생성일: 2026년 10월 27일

Bromine → Ethyl 2-methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-4-carboxylate

https://huagongshe.com/reaction/243662

반응식

참여 물질

역할이름HCID투입량
반응물BromineHCID 24408—
반응물Ethyl 2-oxocyclohexanecarboxylateHCID 95543—
반응물ThioacetamideHCID 2723949—
용매Diethyl EtherHCID 3283—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-4-carboxylateHCID 1291774031%

반응 단계

To a solution of ethyl 2-oxocyclohexanecarboxylate (15 g, 88 mmol) in anhydrous diethyl ether (40 mL) cooled at 0° C. was added bromine (4.5 mL, 88 mmol) dropwise over 15 mins. After complete addition mixture allowed to warm to room temp over 90 min. Mixture diluted with EtOAc (100 mL) and washed with sat. NaHCO3, sat. NaCl, dried over MgSO4, filtered and evaporated. Residue taken up in ethanol (100 mL) and thioacetamide (6.6 g, 88 mmol) added. Mixture stirred at room temp for 1 h then at reflux overnight. Mixture evaporated and residue partitioned between sat. NaHCO3 and DCM. Organic layer dried over MgSO4, filtered and evaporated. Residue purified by MPLC (Biotage Horizon: FLASH 65i) eluent: 100% Hexanes (500 mL), gradient 0 to 25% EtOAc in Hexanes (1200 mL) then 25% EtOAc in Hexanes (1200 mL) to give the title compound (6.14 g, 31%) as a pale orange oil. 1HNMR (500 MHz, CDCl3) δ: 4.22 (q, J=7.1, 2H), 3.84 (t, J=5.5, 1H), 2.80 (m, 1H), 2.73 (m, 1H), 2.65 (s, 3H), 2.18 (m, 1H), 2.11-1.95 (m, 2H), 1.85 (m, 1H), 1.29 (t, J=7.1, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653260B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-59713acd124047149a2bef5418c0c070
출처 메모uspto-grants-2014_02