HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329210Generated: October 30, 2026
Hydrochloric Acid → 2-(Cyclohexylsulfanyl)ethan-1-amine--hydrogen chloride (1/1)
https://huagongshe.com/reaction/329210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyclohexanethiol | HCID 15290 | — |
| Reactant | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(Cyclohexylsulfanyl)ethan-1-amine--hydrogen chloride (1/1) | HCID 21439032 | — |
Reaction Steps
To a solution containing 30 parts of sodium methoxide and 198 parts of methanol, maintained at 25° under a nitrogen atmosphere, is added rapidly 39 parts of cyclohexyl mercaptan. 51 Parts of 2-bromoethylamine hydrobromide then is added portion wise while maintaining the temperature at 25-30°, and the reaction mixture is stirred for 30 minutes. Then the mixture is refluxed for 3 hours, and the solid which forms is separated by filtration and washed with methanol. Residual solvent is removed under reduced pressure to yield a solid which is diluted with water and extracted with ether. The ethereal extracts are dried over a molecular sieve and filtered. The solvent is removed under reduced pressure to afford an oil which is dissolved in anhydrous ether. That solution is cooled in an ice bath while slowly adding isopropanolic hydrochloric acid. The precipitate which forms is recovered by filtration, washed with ether and air dried to afford pure 2-(cyclohexylthio)ethylamine hydrochloride, melting at about 210°-211°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04020079 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-49cb2cc4242549ea850a927029b465d1 |
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| Source note | uspto-grants-1977_04 |
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