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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074015Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 14858911, compound

https://huagongshe.com/reaction/1074015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantDicyclohexylamineHCID 7582—
Reactant1,4-DioxaneHCID 31275—
Reactantepsilon-(Benzyloxycarbonyl)-L-lysineHCID 1715626—
SolventAcetonitrileHCID 6342—
SolventSodium HydroxideHCID 14798—
ProductHCID 14858911HCID 1485891173.2%

Reaction Steps

Nε -benzyloxycarbonyl-L-lysine (8.41 g, 30 mmole) was dissolved in 1N aqueous sodium hydroxide (30 ml), and dioxane (10 ml) solution of benzene sulfonyl chloride (5 30 g, 30 mmole) was added dropwise to the solution while keeping the pH value thereof to between 10 and 11 with 1N aqueous sodium hydroxide while cooling with ice and stirring. The mixture was further stirred for 1.5 hours at room temperature and then insoluble matter was removed by filtration. The filtrate was washed with two 100 ml portions of diethyl ether. To the water layer, ethyl acetate (150 ml) was added and the solution was adjusted to pH 1.5 with 1N aqueous hydrochloric acid under vigorous stirring. The ethyl acetate layer was separated and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the oily residue thus obtained was dissolved in acetonitrile (200 ml), and then dicyclohexylamine (5.43 g, 30 mmole) was added thereto with stirring, and thereby Nα -benzenesulfonyl-Nε -benzyloxycarbonyl-L-lysine dicyclohexylamine salt (13.21 g, 73.2%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971993
Source datasetuspto-grants-1990_11
ORD IDord-9314bd4f8ee4498da2ea1451f6ce536d
Source noteuspto-grants-1990_11