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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420286Generated: November 1, 2026

Hydrochloric Acid → 1,3-dihydro-1-(3-hydroxypropyl)-5-(trifluoromethyl)-2H-benzimidazol-2-one

https://huagongshe.com/reaction/2420286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium cyanateHCID 11378442—
Reactant3-{[2-Amino-4-(trifluoromethyl)phenyl]amino}-1-propanolHCID 20385552—
SolventWaterHCID 962—
Product1,3-dihydro-1-(3-hydroxypropyl)-5-(trifluoromethyl)-2H-benzimidazol-2-oneHCID 2038563434%

Reaction Steps

To a stirred mixture of 21 parts of 3-{[2-amino-4-(trifluoromethyl)phenyl]amino}-1-propanol and 100 parts of water are added 14.4 parts of hydrochloric acid solution. The whole is stirred for 10 minutes at room temperature. After cooling to 0°-10° C, there is added dropwise a solution of 18 parts of potassium cyanate in 50 parts of water. Upon completion, stirring is continued for 2 hours. The precipitated product is filtered off and dried. Then it is melted and the melt is stirred for 10 minutes. After cooling, it is dissolved in trichloromethane while heating. The solution is filtered and the product is allowed to crystallize from the filtrate. It is filtered off and dried, yielding 8 parts (34%) of 1,3-dihydro-1-(3-hydroxypropyl)-5-(trifluoromethyl)-2H-benzimidazol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04110333
Source datasetuspto-grants-1978_08
ORD IDord-fcd68d24fb0647b5a0d74b7508f699e7
Source noteuspto-grants-1978_08