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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074007Generated: October 30, 2026

Benzenesulfonyl chloride → N-benzenesulfonyl-L-prolyl-L-proline benzylester

https://huagongshe.com/reaction/1074007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
ReactantL-prolyl-L-proline benzylester hydrochlorideHCID 14827459—
SolventDichloromethaneHCID 6344—
ProductN-benzenesulfonyl-L-prolyl-L-proline benzylesterHCID 1485886898.1%

Reaction Steps

L-prolyl-L-proline benzylester hydrochloride (1.69 g, 5 mmole) was dissolved in methylene chloride (30 ml), and triethylamine (1.11 g, 11 mmole) was added thereto at -30° C. Methylene chloride (10 ml) solution of benzene sulfonyl chloride (0.86 g, 5 mmole) was added dropwise to the solution. The mixture was stirred for 1 hour at less than 0° C., and next for 5 hours at room temperature, and methylene chloride (60 ml) was added thereto. The solution was washed with 5% aqueous sodium bicarbonate (100 ml, twice), 1N aqueous hydrochloric acid (100 ml, twice) and water (100 ml) in the order given, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain N-benzenesulfonyl-L-prolyl-L-proline benzylester(yield: 2.17 g, 98.1%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971993
Source datasetuspto-grants-1990_11
ORD IDord-834c746514464b538d85ad86b4e593ed
Source noteuspto-grants-1990_11