Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602777Generated: November 1, 2026

Butylamine → 2,6-Dichlorobenzoic acid

https://huagongshe.com/reaction/1602777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylamineHCID 8007—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Dichloro-3-(chlorosulfonyl)benzoic acidHCID 3538216—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
Product2,6-Dichlorobenzoic acidHCID 5758—

Reaction Conditions

Temperature25 °C

Reaction Steps

Part B: 3-(Chlorosulfonyl)-2,6-dichlorobenzoic acid (1.5 g; 5.2 mmol) was dissolved in anhydrous toluene (35 ml) to which was added powdered K2CO3 (1.44 g: 10.4 mmol) and n-butylamine (1.0 ml, 10.4 mmol). The reaction mixture was stirred at 25° C. for 12 hours. The solution was diluted slowly with 1 M ethereal HCl (20 ml) and was then stirred for 30 minutes. The solution was filtered and the resulting filtrate was evaporated to dryness to give crude product. Further purification of the material by silica gel chromatography using EtOAc as the eluent provided 3-N-butylsulfonamidoyl)-2,6-dichlorobenzoic acid (Formula 3) (1.43 g, 85%. 1H NMR (DMSO) d 8.11 (t, 1H), 7.98 and 7.71 (doublets, 1H each), 2.75 (m, 2H), 1.55 (m, 2H), 1.32 (m 2H), 0.87 (t, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05985838
Source datasetuspto-grants-1999_11
ORD IDord-e6357cf367944029b7e2254e2f3077e7
Source noteuspto-grants-1999_11