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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473903Generated: October 30, 2026

Triethylamine → (2-Bromopyridin-3-yl)methanol

https://huagongshe.com/reaction/1473903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2-Bromopyridine-3-carboxylic acidHCID 233262—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2-Bromopyridin-3-yl)methanolHCID 1476146090.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-bromonicotinic acid (4.0 g, 20 mmol) and triethylamine (3.34 mL, 24 mmol, 1.2 eq.) in THF (100 mL) was added i-butyl chloroformate (3.12 mL, 24 mmol, 1.2 eq.) at 0° C. The mixture was stirred at 0° C. for 10 min and filtered. To this filtrate was added a suspension of NaBH4 (1.52 g, 40 mmol, 2 eq.) in water (1.0 mL) at 0° C. The mixture was stirred for 30 min, added water (3 mL), continued to stir for 2 h, and concentrated to dryness. The crude was purified on silica gel using a mixture of ethylacetate and hexanes as eluent to give (2-bromopyridin-3-yl)methanol (3.4 g, 90%) as a white solid. LRMS (M+H+) m/z 188.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018210B2
Source datasetuspto-grants-2015_04
ORD IDord-f8cf047a6c194398bba655cb354ad5c3
Source noteuspto-grants-2015_04