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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110812Generated: November 3, 2026

2-Methoxyaniline → HCID 10803061, compound

https://huagongshe.com/reaction/1110812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyanilineHCID 7000—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 14856792HCID 14856792—
SolventDichloromethaneHCID 6344—
ProductHCID 10803061HCID 1080306137%

Reaction Conditions

Temperature90 °C

Reaction Steps

Thionyl chloride, 5 ml, was added to 0.50 g (0.97 mmols) of 2-methyl-4,5,6,7-tetrahydrobenzimidazole-5carboxylic acid hydrochloride (including 58 w/w % of NaCl) obtained in Reference Example 2 and the mixture was heated at 90° C. for 3 hours. After thionyl chloride was distilled off under reduced pressure, 10 ml of methylene chloride was added to the residue and at 0° to 5° C., 0.20 ml (1.78 mmol) of o-anisidine and 0.40 ml (2.89 mmols) of triethylamine were added to the mixture followed by stirring at room temperature for 16 hours. After 50 ml of methylene chloride was supplemented, the mixture was washed with 1 N sodium hydroxide solution and then dried over anhydrous magnesium sulfate, the solvent was distilled off. The residue was subjected to silica gel column chromatography and eluted with methylene chloride-methanol-ammonia water (10 : 1 : 0.1). The solvent was distilled off and the resulting colorless crystals were recyrstallized from ethyl acetate to give 0.10 g (37.0%) of N-(2-methyoxyphenyl)-2-methyl -4,5,6,7-tetrahydrobenzimidazole-5-carboxamide monhydrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977175
Source datasetuspto-grants-1990_12
ORD IDord-7c3eddef3a504461af47ee140d43c793
Source noteuspto-grants-1990_12