HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463540Generated: October 23, 2026
Hydrochloric Acid → hexamethylene bis(thiosulphate)N-tert-butyl-N-benzylammonium salt
https://huagongshe.com/en/reaction/463540
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thiosulfate ion | HCID 1084 | — |
| Reactant | Sodium Thiosulfate Pentahydrate | HCID 61475 | — |
| Reactant | Cyclohexane, 1,4-bis(chloromethyl)- | HCID 69992 | — |
| Reactant | N-(1,1-Dimethylethyl)benzenemethanamine | HCID 76908 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | hexamethylene bis(thiosulphate)N-tert-butyl-N-benzylammonium salt | HCID 131714228 | — |
Reaction Steps
1,4-bis(chloromethyl)cyclohexane (0.165 mole), sodium thiosulphate pentahydrate (0.369 mole) sodium sulfite (6.1 g), methanol (150 ml) and water (150 ml) were charged into an autoclave and heated at 135° C. for 45 minutes. To the cooled reaction mixture, which was a solution of 1,4-dimethylcyclohexane-α,α-bis(thiosulphate)sodium salt, 400 ml of water was added. N-tert-butylbenzylamine (0.306 mole) in 150 ml methanol and 850 ml H2O was adjusted with concentrated HCl to pH4, and the resulting solution was added with stirring to the thiosulphate solution. The white precipitate was filtered, washed with water and dried. Yield: 92 g, (91%) of 1,4-dimethylcyclohexane-α,α-bis(thiosulphate)N-tert-butyl, N-benzylammonium salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04520154 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-32b8be04b6174a2580d656012a7d1254 |
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| Source note | uspto-grants-1985_05 |
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