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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894366Generated: October 29, 2026

Benzhydrylamine → 3-Chloro-propane-1-sulfonic acid benzhydryl-amide

https://huagongshe.com/reaction/1894366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrylamineHCID 7036—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
SolventWaterHCID 962—
Product3-Chloro-propane-1-sulfonic acid benzhydryl-amideHCID 43653836118.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a three-neck round bottom flask equipped with argon inlet was charged with anhydrous tetrahydrofuran and 3-chloropropane sulfonyl chloride (500 mg, 2.82 mmol, Aldrich). The flask was cooled down to 0° C., and aminodiphenylmethane (0.49 mL, 2.82 mmol, Fluka) was added, followed by triethylamine (0.59 mL, 4.23 mmol). The reaction mixture was stirred at 0° C. and monitored by the thin layer chromatography. Upon completion, water was added the reaction mixture. It was concentrated then diluted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated to give 3-chloro-propane-1-sulfonic acid benzhydryl-amide (1.083 g, light brown solid). The crude product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513239B2
Source datasetuspto-grants-2013_08
ORD IDord-34c7f4a9864a49a5bc04c5f02675cac3
Source noteuspto-grants-2013_08