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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071849Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 5314675, compound

https://huagongshe.com/reaction/1071849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
ReactantPiperonylamineHCID 2723901—
SolventDichloromethaneHCID 6344—
ProductHCID 5314675HCID 531467583.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-piperidone monohydrate hydrochloride (4.59 g, 30 mmol), triethylamine (12.5 ml, 90 mmol) in CH2Cl2 (50 ml) was added benzenesulfonyl chloride (5.30 g, 30 mmol). The mixture was stirred at 25° C. for 16 h. After evaporation of solvents, the residue was triturated with water (100 ml), filtered, and further purified by recrystallization from hexanes/CH2Cl2 (3:1) to afford the desired ketone (5.97 g, 83%) as a colorless solid. mp 116-118° C.; 1H NMR (500 MHz, CDCl3) δ2.54 (t, J=6.4 Hz, 4H), 3.41(t, J=6.4 Hz, 4H). 7.58 (d, J=7.8 Hz, 2H), 7.63 (t, J=7.0 Hz, 1H), 7.81 (d, J=7.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906205B2
Source datasetuspto-grants-2005_06
ORD IDord-edc3193c680842d499dcae586a28e0c9
Source noteuspto-grants-2005_06