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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165757Generated: October 30, 2026

Hydrochloric Acid → (2-Bromopyridin-4-yl)methanol

https://huagongshe.com/reaction/1165757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron trifluoride etherateHCID 8000—
Reactant2-Bromoisonicotinic acidHCID 222701—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178418361HCID 178418361—
SolventTetrahydrofuranHCID 8028—
Product(2-Bromopyridin-4-yl)methanolHCID 1451295788.6%

Reaction Steps

17.4 g of sodium borohydride was suspended in 1.6 liters of tetrahydrofuran, and the suspension was stirred by a mechanical stirrer. The suspension was cooled with ice-water, and 62.2 g of 2-bromo-4-pyridinecarboxylic acid was added little by little. The mixture was heated to room temperature, and stirred until evolution of hydrogen ceased. A solution of 75.8 ml of boron trifluoride etherate in 500 ml of tetrahydrofuran was added dropwise at room temperature for 3 hours. After the addition, the mixture was stirred for 20 hours. The reaction solution was cooled with ice-water, and acidified to a pH of 1 to 2 by adding 1.5N hydrochloric acid. Tetrahydrofuran was evaporated under reduced pressure. A 4N aqueous solution of sodium hydroxide was added to adjust the pH of the mixture to 10 to 11. It was extracted with ethyl acetate, and the organic layer was washed with a saturated aqueous solution of sodium chloride. The aqueous layer was further extracted with ethyl acetate twice. The organic layers were combined, and dried over anhydrous sodium sulfate. The dried product was concentrated under reduced pressure to give 51.3 g of 2-bromo-4-pyridinemethanol in a yield of 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04912101
Source datasetuspto-grants-1990_03
ORD IDord-c386aad5aad64658b846aeaab7598d6c
Source noteuspto-grants-1990_03