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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanogen Chloride | HCID 10477 | — |
| Reactant | 2-mercaptobenzoic acid N-(3,5,5-trimethyl-cyclohexyl)-amide | HCID 13503961 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-thiocyanato-benzoic acid N-(3,5,5-trimethylcyclohexyl)-amide | HCID 13503965 | 86.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04565829 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-298bddfa3f4349dba27ac7936e4cb3e9 |
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| Source note | uspto-grants-1986_01 |
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