Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500345Generated: November 2, 2026

Sodium borohydride → (4-(2-Fluorophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)methanol

https://huagongshe.com/reaction/1500345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2-Fluorophenyl)-1-methyl-1H-1,2,3-triazole-5-carbaldehydeHCID 86664762—
SolventMethanolHCID 887—
Product(4-(2-Fluorophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)methanolHCID 6749821080.8%

Reaction Steps

To a stirred solution of 4-(2-Fluorophenyl)-1-methyl-1H-1,2,3-triazole-5-carbaldehyde 4 (38 g, 185.19 mmol) under nitrogen atmosphere in methanol (300 ml) was added sodium borohydride (8.407 g, 222.23 mmol) in portion wise at 0° C. and the reaction mass stirred for 20 min. The reaction was monitored by TLC and UPLC. The reaction mixture was quenched with water (500 ml) and concentrated to remove methanol and water. Then it was extracted with ethyl acetate (4×500 ml), combined organic layer was washed with brine (50 ml), dried over sodium sulphate, filtered and concentrated to afford crude mass (34 g, 88.6% mass balance). The above solid was triturated with hexane (3×100 ml), the supernant layer was decanted and the solid was dried to afford desired product (4-(2-Fluorophenyl)-1-methyl-1H-1,2,3-triazole-5-yl) methanol (31 g, 80.77%) as off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206160B2
Source datasetuspto-grants-2015_12
ORD IDord-00d6430ebd5a4b9ca4b2d92d562ab3a7
Source noteuspto-grants-2015_12