Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327427Generated: October 31, 2026

Oxalyl chloride → 1-Methyl-4-nitro-1H-imidazole-2-carbonyl chloride

https://huagongshe.com/reaction/327427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-Methyl-4-nitro-1H-imidazole-2-carboxylic acidHCID 12067998—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-4-nitro-1H-imidazole-2-carbonyl chlorideHCID 19108629—

Reaction Steps

To a suspension of 1-methyl-4-nitroimidazole-2-carboxylic acid (3.00 g, 17.5 mmol) in dry THF (30 mL) was slowly added oxalyl chloride (12 mL). The reaction mixture was heated to reflux under a drying tube for 45 minutes at which time the excess oxalyl chloride and THF were removed under reduced pressure and the acid chloride coevaporated twice with dry CH2Cl2 (20 mL each) yielding 1-methyl-4-nitroimidazole-2-carbonyl chloride as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273991
Source datasetuspto-grants-1993_12
ORD IDord-c4c400ae5f8048268425aac0e1979e00
Source noteuspto-grants-1993_12