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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437137Generated: November 1, 2026

Ammonium Chloride → (1-methyl-1H-1,2,3-triazol-4-yl)methanamine hydrochloride

https://huagongshe.com/reaction/1437137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium borohydrideHCID 4148881—
Reactant1-Methyl-1H-1,2,3-triazole-4-carboxamideHCID 21828989—
SolventMethanolHCID 887—
SolventDiglymeHCID 8150—
Product(1-methyl-1H-1,2,3-triazol-4-yl)methanamine hydrochlorideHCID 69061589—

Reaction Conditions

Temperature155 °C

Reaction Steps

A solution of 1-methyl-1H-1,2,3-triazole-4-carboxamide (Bull. Chem. Soc. Jap. (1972), 45(8), 2577-9) (0.050 g) in bis(2-methoxyethyl)ether (diglyme, 2 ml) was treated with lithium borohydride (0.0264 g) and heated to reflux (oil bath 155° C.). Methanol (0.18 ml) was added dropwise in two portions after 5 min and 35 min, and the mixture heated under reflux for 1.5 h with stirring under nitrogen. Saturated aqueous ammonium chloride (0.2 ml) was added dropwise to the cooled mixture, and the mixture was diluted with methanol (2 ml). The solution was applied directly to an Isolute SCX ion exchange cartridge (5 g) (pre-eluted with methanol) and eluted with methanol followed by 10% 0.880 ammonia in methanol. The ammonia in methanol fraction was evaporated to low volume (ca. 1 ml), acidified with 4N hydrogen chloride in 1,4-dioxane (1 ml), and evaporated to dryness in vacuo to give the title compound (0.030 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622464B2
Source datasetuspto-grants-2009_11
ORD IDord-d3d9131becee4ec497a74d6e11e82b68
Source noteuspto-grants-2009_11