Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197642Generated: October 31, 2026

2-Aminoheptane → HCID 19107601, compound

https://huagongshe.com/reaction/1197642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminoheptaneHCID 5603—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(Bromomethyl)benzenesulfonyl chlorideHCID 2734409—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19107601HCID 1910760139%

Reaction Steps

To a solution of 2-aminoheptane (1.67 ml, 0.011 mol) and triethylamine (1.55 ml, 0.011 mol) in dry THF (100 ml) was added powdered 4-bromomethylbenzenesulphonyl chloride (3.0 g, 0.011 mol) in one portion. The mixture was stirred for 3 h at room temperature. The reaction mixture was treated with saturated ammonium chloride (60 ml) , extracted with ethyl acetate (3×80 ml), the organics combined and washed with water (50 ml) and brine (50 ml), dried over anhydrous sodium sulphate, filtered and evaporated. The resulting oil was purified by chromatography (silica: 1:2 hexane:ethyl acetate) to give N-1-methylhexyl 4-bromomethylbenzenesulphonamide (1.45 g, 39%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276153
Source datasetuspto-grants-1994_01
ORD IDord-656734927bcc42ed9c24534f1ac78f56
Source noteuspto-grants-1994_01