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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375197Generated: November 1, 2026

4-Chlorobenzenesulfonyl chloride → HCID 25263461, compound

https://huagongshe.com/reaction/1375197

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantTriethylamineHCID 8471—
Reactant(2S)-2-Amino-3,3-dimethyl-1-butanolHCID 2734079—
SolventDichloromethaneHCID 6344—
ProductHCID 25263461HCID 25263461—

Reaction Steps

To a solution of S-tert-leucinol (0.20 g, 1.70 mmol), triethylamine (0.19 g, 1.87 mmol) and methylene chloride (10 mL) at 0° C., was added a solution of 4-chloro benzenesulfonyl chloride (0.36 g, 1.70 mmol) in CH2Cl2 (5 mL). After 15 minutes the ice bath was removed and the reaction allowed to reach 25° C. After 16 hours, the reaction was quenched by pouring into saturated sodium bicarbonate solution (20 mL) and additional-methylene chloride (15 mL). The organic phase was separated and washed sequentially with 1N HCl solution (20 mL), distilled water and brine, dried over MgSO4 and evaporated to give the desired product as a white solid, mp 128-130° C. (0.46 g, 94%). MS (+APCI) 292.06 ([M+H]+). Anal. Calc'd for C12H18ClNO3S: C, 49.39; H, 6.22; N, 4.80; Found: C, 49.40; H, 6.17; N, 4.79.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166622B2
Source datasetuspto-grants-2007_01
ORD IDord-c9baa03ff36e4b3b85af6cf280c51b1d
Source noteuspto-grants-2007_01