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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332010Generated: October 28, 2026

Triethylamine → (5-Methyl-3-pyrimidin-4-yl-isoxazol-4-yl)-methanol

https://huagongshe.com/reaction/332010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Methyl-3-pyrimidin-4-yl-isoxazole-4-carboxylic acidHCID 67157819—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product(5-Methyl-3-pyrimidin-4-yl-isoxazol-4-yl)-methanolHCID 6715842619%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 5-methyl-3-pyrimidin-4-yl-isoxazole-4-carboxylic acid (300 mg, 1.46 mmol) in THF (4 mL) at −10° C. was added triethylamine (203 μL, 1.46 mmol) and then a solution of ethylchloroformate (139 μL, 1.46 mmol) in THF (1 mL) added keeping the temperature below −5° C. After 1 h the mixture was filtered and the filtrate cooled to −10° C. and a suspension of sodiumborohydride (138 mg, 3.66 mmol) in water (1.5 mL) added over 15 minutes keeping the temperature below −5° C. The mixture was then allowed to warm up to room temperature over 2 h and diluted with aqueous sodium hydroxide (1 N) and extracted with ethylacetate. The combined organic layers were then washed with water and brine, dried over sodium sulfate and evaporated. Purification by chromatography (SiO2, dichloromethane:methanol=9:1) afforded the title product (52.5 mg, 19%) which was obtained as white solid. MS: m/e=190.0 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877782B2
Source datasetuspto-grants-2014_11
ORD IDord-8cb6e1ce2b74468dbde0bc7bd14a980c
Source noteuspto-grants-2014_11