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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166059Generated: October 31, 2026

Acetic Acid → HCID 14990857, compound

https://huagongshe.com/reaction/2166059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantHCID 14990746HCID 14990746—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductHCID 14990857HCID 1499085749%

Reaction Steps

A mixture of 1.6 parts of 4-(1H-imidazol-1-ylmethyl)-N2 -phenyl-1,2-benzenediamine, 20 parts of acetic acid and 1.08 parts of concentrated hydrochloric acid was cooled in an ice bath at 12°-16° C. A solution of 0.83 parts of sodium nitrite in 7 parts of water was added dropwise. Upon complete addition, the reaction mixture was allowed to reach room temperature while stirring. The reaction mixture was poured into alkaline ice water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel first using a mixture of trichloromethane and methanol, saturated with ammonia, (97.5:2.5 by volume) and then a mixture of ethyl acetate, methanol and methanol, saturated with ammonia (92:2.5:2.5 by volume) as eluents. The pure fractions were collected and the eluent was evaporated. The residue was taken up in a mixture of 2-propanone and 2,2'-oxybispropane. The product was filtered off, washed with 2,2'-oxybispropane and dried in vacuo at 60° C., yielding 0.81 parts (49.0%) of 6-(1H-imidazol-1-ylmethyl)-1-phenyl-1H-benzotriazole; mp. 110.1° C. (compound 72).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943574
Source datasetuspto-grants-1990_07
ORD IDord-be93a180c7b04a4faabc4246f886db67
Source noteuspto-grants-1990_07