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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285146Generated: October 26, 2026

Cyanogen Chloride → 2-thiocyanato-benzoic acid N-(3,5,5-trimethylcyclohexyl)-amide

https://huagongshe.com/reaction/1285146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen ChlorideHCID 10477—
Reactant2-mercaptobenzoic acid N-(3,5,5-trimethyl-cyclohexyl)-amideHCID 13503961—
SolventTetrahydrofuranHCID 8028—
Product2-thiocyanato-benzoic acid N-(3,5,5-trimethylcyclohexyl)-amideHCID 1350396586.5%

Reaction Conditions

Temperature-15 °C

Reaction Steps

49.9 g (0.18 mol) of 2-mercaptobenzoic acid N-(3,5,5-trimethyl-cyclohexyl)-amide are initially introduced into 200 ml of tetrahydrofuran. The solution is cooled to -15° C. and 33.3 g (0.54 mol) of cyanogen chloride, dissolved in 50 ml of tetrahydrofuran, are added dropwise in the course of 30 minutes such that the internal temperature does not exceed -5° C. When the dropwise addition has ended, the mixture is allowed to come to room temperature in the course of 1 hour and stirring is then continued at this temperature for a further 2 hours. Excess cyanogen chloride and some of the solvent are distilled off under reduced pressure. The solution is poured into water, with vigorous stirring, and the solid which has precipitated is filtered off with suction and dried in a desiccator. 47 g (86.5% of theory) of 2-thiocyanato-benzoic acid N-(3,5,5-trimethylcyclohexyl)-amide are obtained as a colorless powder of melting point 117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04565829
Source datasetuspto-grants-1986_01
ORD IDord-298bddfa3f4349dba27ac7936e4cb3e9
Source noteuspto-grants-1986_01