Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567945Generated: October 26, 2026

Hydrochloric Acid → HCID 54571482, compound

https://huagongshe.com/reaction/567945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactantepsilon-(Benzyloxycarbonyl)-L-lysineHCID 1715626—
SolventDichloromethaneHCID 6344—
ProductHCID 54571482HCID 54571482—

Reaction Steps

(S)-N6-Benzyloxycarbonyllysine (1.5 kg) was slurried in methylene chloride (7.5 l) and chlorotrimethylsilane (1.36 l) added over 10 minutes. The mixture was heated under reflux for 30 minutes to give a solution which was cooled to 3° C. before simultaneously adding diisopropylethylamine (1.87 l) and methanesulphonyl chloride (435 ml) at such a rate as to keep the temperature below 25° C. The reaction was stirred for a further 2.5 hours then poured into 2 M aqueous hydrochloric acid solution. The layers were separated and the methylene chloride phase was washed with 2 M aqueous hydrochloric acid solution followed by water. The solvent was removed under reduced pressure and replaced with n-butyl acetate. The solution was cooled and the resulting crystalline material was collected by filtration, washed with n-butyl acetate and dried under reduced pressure to provide the title compound (1.63 kg), m.p. 83.5-84° C. [α]D25−13.4° (c=1, methanol). Found: C,50.23; H,6.40; N,7.76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180665B2
Source datasetuspto-grants-2001_01
ORD IDord-ceff208f793f4ad1beba14b01695d80b
Source noteuspto-grants-2001_01