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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThiosulfate ionHCID 1084—
ReactantSodium Thiosulfate PentahydrateHCID 61475—
ReactantCyclohexane, 1,4-bis(chloromethyl)-HCID 69992—
ReactantN-(1,1-Dimethylethyl)benzenemethanamineHCID 76908—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Producthexamethylene bis(thiosulphate)N-tert-butyl-N-benzylammonium saltHCID 131714228—

Reaction Conditions

Temperature135 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04520154
Source datasetuspto-grants-1985_05
ORD IDord-32b8be04b6174a2580d656012a7d1254
Source noteuspto-grants-1985_05