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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251407Generated: November 2, 2026

Tert-Butylamine → HCID 86602999, compound

https://huagongshe.com/reaction/2251407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantHCID 23106070HCID 23106070—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86602999HCID 86602999—

Reaction Steps

70.0 ml (736 mmol) of tert-butylamine are used as initial charge in 1,2-dichloroethane in an inertized three-necked flask with dropping funnel, reflux condenser with hose coupling at its upper end, a tap with hose coupling and a Teflon stirrer bar, in a countercurrent of argon. 10.2 g (29.3 mmol) of 1,6-bis(chlorotrisulphanyl)hexane in 50 ml of 1,2-dichloroethane are then added dropwise, with stirring. The reaction mixture is stirred at room temperature for 4 hours. The resultant salt is filtered off, and the organic phase is washed three times with water and dried over sodium sulphate. After removal of the solvent on a rotary evaporator and drying in the vacuum generated by a rotary-vane pump, 1,6-bis(tert-butylaminotrisulphanyl)hexane precipitates in the form of a yellow oil. The crude yield is 11.9 g (97%). Elemental analysis was carried out on the crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319124B2
Source datasetuspto-grants-2008_01
ORD IDord-55f478889cea4517bfa5d15d5b4c68df
Source noteuspto-grants-2008_01