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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239305Generated: October 31, 2026

Methanol → Methyl 4-(Benzyloxy)-2-methyl-1H-benzo[d]imidazole-6-carboxylate

https://huagongshe.com/reaction/2239305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant4-(benzyloxy)-2-methyl-1H-benzo[d]imidazole-6-carboxylic acidHCID 68574531—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-(Benzyloxy)-2-methyl-1H-benzo[d]imidazole-6-carboxylateHCID 68577093—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-methyl-4-[(phenylmethyl)oxy]-1H-benzimidazole-6-carboxylic acid (10.0 g, 35.4 mmol, STEP 4 in Example 1), and thionyl chloride (5.2 mL, 7.1 mmol) in methanol (300 mL) was stirred at 80° C. for 3 hours. The mixture was diluted with ethyl acetate, and washed with saturated ammonium chloride aqueous solution. The organic layer was dried over magnesium sulfate, and concentrated in vacuum. The residue was diluted with methanol, filtered to remove the precipitate, and the filtrate was concentrated in vacuum. The resulted solid was washed with dichloromethane to give the title compound as a brown solid (29.8 g, crude), which was used in the next step without further purification. MS (ESI) m/z: 297 (M+H)+, 295 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723321B2
Source datasetuspto-grants-2010_05
ORD IDord-7c690e24aec949af9893321babf744d2
Source noteuspto-grants-2010_05