Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293733Generated: October 30, 2026

Semicarbazide hydrochloride → 6-[(2-chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-alpha-methyl-1H-benzotriazole-1-acetaldehyde semicarbazone

https://huagongshe.com/reaction/2293733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSemicarbazide hydrochlorideHCID 11236—
ReactantSodium AcetateHCID 517045—
Reactant6-[(2-chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl) oxy]-alpha-methyl-1H-benzotriazol-1-acetaldehydeHCID 86747948—
SolventEthanolHCID 702—
Product6-[(2-chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-alpha-methyl-1H-benzotriazole-1-acetaldehyde semicarbazoneHCID 86747947—

Reaction Steps

A mixture of 6-[(2-chloro-α,α,α,6-tetrafluoro-p-tolyl)oxy]-α-methyl-1H-benzotriazole-1-acetaldehyde (0.0295 mole), semicarbazide hydrochloride (4.0 g, 0.035 mole), and sodium acetate (5.8 g, 0.071 mole) in aqueous ethanol is heated to reflux temperature, cooled and filtered. The solid filter cake is recrystallized from ethanol to give the title compound as a solid, mp 170°-171° C., identified by elemental and NMR analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686617
Source datasetuspto-grants-1997_11
ORD IDord-a1f76f334e8244129f5638e83708baff
Source noteuspto-grants-1997_11