HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848789Generated: October 25, 2026
Hydrochloric Acid → 1-Amino-3,6-dithianonane
https://huagongshe.com/reaction/848789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Carbamimidothioic acid, 10-undecenyl ester, monohydriodide | HCID 31429 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Chloroethylamine hydrochloride | HCID 9793737 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Amino-3,6-dithianonane | HCID 20564652 | — |
Reaction Steps
76.4 g (0.164 mole) of 1-hydroxy-3-thiahexane, produced from propane-1-thiol and 2-chloroethanol in the presence of the equivalent quantity of sodium hydroxide were boiled under reflux for 2 hours with 50 g of thiourea and 77 g of 37% hydrochloric acid. After cooling, 32 g (0.8 mole) of sodium hydroxide in 60 ml of water were added to the clear solution of the isothiuronium salt. Thereafter the mixture was heated for 30 minutes on a steam bath. The 1-mercapto-3-thiahexane precipitated was separated off in a separation funnel and was dissolved under nitrogen in a solution of 68 g (1.7 moles) of sodium hydroxide in 130 ml of water accommodated in a three-necked flask. A total of 74.5 g of 2-chloroethylamine hydrochloride in 200 ml of water was added dropwise to the resulting solution at 333° K. After 1 hour on a steam bath, the amine phase precipitated was separated off with ether (300 ml), dried with 40 g of KOH flakes, concentrated by evaporation and fractionated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04297439 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-1c0d239cadd6416db2e7deb6dc93983e |
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| Source note | uspto-grants-1981_10 |
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