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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195614Generated: November 2, 2026

Triethylamine → Ethyl 2-(4-butoxyphenyl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/1195614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 3614036HCID 3614036—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
SolventHCID 178418361HCID 178418361—
ProductEthyl 2-(4-butoxyphenyl)pyrimidine-5-carboxylateHCID 1390740880%

Reaction Steps

This compound (V) (3.3 g, 10 mmols) was dissolved in ethyl acetate (30 ml), followed by agitating the solution together with Pd/C (5%) (0.6 g) and triethylamine (1.0 g) in hydrogen atmosphere at room temperature for 3 hours, filtering off Pd/C, adding toluene (100 ml), washing the resulting fluid with 2N-hydrochloric acid (50 ml), washing it with water till the washing water became pH 7, drying the toluene phase over anhydrous magnesium sulfate, filtering off magnesium sulfate, concentrating under reduced pressure to obtain white crystals and recrystallizing the crystals from methanol to obtain ethyl-2-(4-butyloxyphenyl)-5-pyrimidinecarboxylate (VI) (2.4 g) (yield: 80%) having a melting point 99.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112523
Source datasetuspto-grants-1992_05
ORD IDord-df3701453e05455f9bfd5954154153f1
Source noteuspto-grants-1992_05