Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889566Generated: October 25, 2026

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

https://huagongshe.com/reaction/889566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
Reactant3,3-Diethoxy-1-propeneHCID 62477—
Reactant3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acidHCID 66938857—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid ethyl esterHCID 6693834166.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252830B2
Source datasetuspto-grants-2012_08
ORD IDord-6fb84f37688549b48cd5799e5df8c943
Source noteuspto-grants-2012_08