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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12514Generated: October 26, 2026

3-Chlorobenzenesulphonyl chloride → HCID 178464646, compound

https://huagongshe.com/reaction/12514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzenesulphonyl chlorideHCID 17909—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178464603HCID 178464603—
SolventDichloromethaneHCID 6344—
ProductHCID 178464646HCID 178464646—

Reaction Steps

6.39 g N-Ethyl-4,4-dimethyl-4,5-dihydro-pyrazole-1-carboxamidine hydrochloride was suspended in 65 mL DCM. 12.0 mL DIPEA and 3.96 mL 3-chloro-benzenesulfonyl chloride were added and the suspension was stirred for 20 h. at room temperature, resulting in a dark brown turbid solution. The mixture was extracted with 2M NaOH (2×125 mL) and 1M HCl (2×125 mL)7 washed with water (100 mL), and the organic layer was dried over Na2SO4 followed by evaporation under reduced pressure to yield 7.70 g of a brown oil. The oil (1.0 g) was dissolved in MTBE (3 mL) under reflux, and the solution was slowly cooled to room temperature, initializing crystallization The suspension was stirred for 10 min at room temperature, hexane (6 mL) was added over a period of 1 minute. The resulting suspension was stirred for 20 min. at room temperature and 50 min. at 0° C., and product was collected by filtration and washed with hexane (1 mL). Drying under reduced pressure at 40° C. yielded 0.85 g of a light-brown solid, m.p. 62-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728018B2
Source datasetuspto-grants-2010_06
ORD IDord-f74a5cfdc3c645d594fa518fd94b6452
Source noteuspto-grants-2010_06