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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248348Generated: October 29, 2026

Hydrochloric Acid → HCID 178420196, compound

https://huagongshe.com/reaction/2248348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 14990935HCID 14990935—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178420196HCID 17842019679.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 5.85 parts of 6-[phenyl(1H-1,2,4-triazol-1-yl)methyl]-1H-benzotriazol-1-ol, 1.4 parts of potassium carbonate and 27.5 parts of dimethyl sulfoxide was stirred for 30 minutes at 50° C. After cooling, 3.55 parts of ethyl 2-bromoacetate were added and the whole was stirred for 2 hours at room temperature. Another portion of 1.4 parts of potassium carbonate was added. After stirring for 3 hours at 50° C., the mixture was cooled and 2.0 parts of concentrated hydrochloric acid were added. The dimethyl sulfoxide layer was evaporated. The residue was taken up in 25 parts of water and 130 parts of dichloromethane. The separated organic layer was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane, methanol and methanol, saturated with ammonia, (92:4:4 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 20 parts of 4-methyl-2-pentanone. The product was filtered off and dried, yielding 4.4 parts (79.6%) of 5-[phenyl(1H-1,2,4-triazol-1-yl)methyl]-1H-benzotriazole; mp. 182.7° C. (compound 230).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039677
Source datasetuspto-grants-1991_08
ORD IDord-abc8055151d348b1a78d6607c8cc94ff
Source noteuspto-grants-1991_08