Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465554Generated: November 1, 2026

Triphenylphosphine → 4-[4-(p-Chlorophenylsulfonamido)butyl)-epsilon-caprolactone

https://huagongshe.com/reaction/465554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-ChlorobenzenesulfonamideHCID 66824—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant5-(4-Hydroxybutyl)oxepan-2-oneHCID 10330069—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-[4-(p-Chlorophenylsulfonamido)butyl)-epsilon-caprolactoneHCID 10361132—

Reaction Steps

To a solution of 3.53 g of 4-(4-hydroxybutyl)-epsilon-caprolactone in 14 ml methylene chloride and 14 ml tetrahydrofuran is added 4.24 g p-chlorophenylsulfonamide followed by 7.44 g triphenylphosphine. The reaction mixture is stirred at room temperature for 0.5 h and then 6.1 ml diethyl azodicarboxylate is added slowly with cooling. After the addition, the cooling bath is removed and the solution is stirred at room temperature overnight. The reaction mixture is evaporated to dryness to yield 4-[4-(p-chlorophenylsulfonamido)butyl)-epsilon-caprolactone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153214
Source datasetuspto-grants-1992_10
ORD IDord-82aaf2a46a714d7e8ebfb5170c20d777
Source noteuspto-grants-1992_10