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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 463540Erstellt: 24. Oktober 2026

Hydrochloric Acid → hexamethylene bis(thiosulphate)N-tert-butyl-N-benzylammonium salt

https://huagongshe.com/de/reaction/463540

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktThiosulfate ionHCID 1084—
EduktSodium Thiosulfate PentahydrateHCID 61475—
EduktCyclohexane, 1,4-bis(chloromethyl)-HCID 69992—
EduktN-(1,1-Dimethylethyl)benzenemethanamineHCID 76908—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkthexamethylene bis(thiosulphate)N-tert-butyl-N-benzylammonium saltHCID 131714228—

Reaktionsbedingungen

Temperatur135 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04520154
Quelldatensatzuspto-grants-1985_05
ORD IDord-32b8be04b6174a2580d656012a7d1254
Quellennotizuspto-grants-1985_05