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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1911703생성일: 2026년 10월 26일

Tributylamine → 3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid ethyl ester

https://huagongshe.com/reaction/1911703

반응식

참여 물질

역할이름HCID투입량
반응물TributylamineHCID 7622—
반응물3,3-Diethoxy-1-propeneHCID 62477—
반응물3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acidHCID 66938857—
촉매Tetrabutylammonium ChlorideHCID 70681—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid ethyl esterHCID 6693834166.8%

반응 조건

온도90 °C

반응 단계

3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid: To a mixture of 117A (956 mg, 4.00 mmol), 3,3-diethoxyprop-1-ene (1562 mg, 12.00 mmol), and Bu4NCl (1110 mg, 4.00 mmol) in DMF (22 mL) was added Bu3N (1480 mg, 8.00 mmol). To this mixture under N2 was added Pd(OAc)2 (26.9 mg, 0.12 mmol). The resulting mixture was stirred at 90° C. for 1.5 h, then cooled to rt and quenched with 2N HCl (10 mL). The resulting mixture was stirred for 20 min, then evaporated. The mixture was diluted with EtOAc, washed with water and brine, dried over MgSO4, and purified by flash chromatography to provide 3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid ethyl ester (695 mg, 66.8%). LCMS m/z 261.2 (M+H)+. To a solution of this intermediate (690 mg, 2.65 mmol), in THF (10 mL) was added 2N LiOH (10 mL). The resulting mixture was stirred at rt for 3 h, then acidified to pH 3-4 with 2N HCl at 0° C. The mixture was concentrated and extracted with EtOAc (5×20 mL). The combined organic layers were washed with brine, dried over MgSO4, and purified by prep. HPLC to give 117B (567 mg, 92%). LCMS m/z 233.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08604056B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-2793b045dbb04492a06312c17e14e888
출처 메모uspto-grants-2013_12