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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402365Generated: October 30, 2026

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

https://huagongshe.com/reaction/402365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
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 6749821087%

Reaction Steps

To a solution of 4-(2-fluorophenyl)-1-methyl-1H-1,2,3-triazole-5-carbaldehyde (411 mg, 2.0 mmol) in MeOH (42 mL) was added sodiumborohydride (38 mg, 1.00 mmol) under Argon at room temperature and the reaction mixture was allowed to warm up to room temperature over 0.5 h. The mixture was then poured into saturated ammonium chloride solution and extracted with ethyl acetate and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated. Purification by chromatography (silica, 0 to 100% ethyl acetate in heptane) afforded the title compound (360 mg, 87%) as a white solid. MS: m/e=208.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742097B2
Source datasetuspto-grants-2014_06
ORD IDord-2ef7107854bd4bacb7c315e16d79adee
Source noteuspto-grants-2014_06