Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465616Generated: October 29, 2026

ethyl 8-[N-(p-chlorophenylsulfonyl)-N-(t-butoxycarbonyl)-amino]-4-[2-(3-pyridyloxy)ethyl]-octanoate → Ethyl 8-(p-chlorophenylsulfonamido)-4-[2-(3-pyridyloxy)ethyl]octanoate

https://huagongshe.com/reaction/465616

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 8-[N-(p-chlorophenylsulfonyl)-N-(t-butoxycarbonyl)-amino]-4-[2-(3-pyridyloxy)ethyl]-octanoateHCID 14986717—
SolventTrifluoroacetic acidHCID 6422—
ProductEthyl 8-(p-chlorophenylsulfonamido)-4-[2-(3-pyridyloxy)ethyl]octanoateHCID 14986718—

Reaction Steps

A solution of 2.9 g (5 mmol) of ethyl 8-[N-(p-chlorophenylsulfonyl)-N-(t-butoxycarbonyl)-amino]-4-[2-(3-pyridyloxy)ethyl]-octanoate in 30 ml trifluoroacetic acid is stirred at room temperature. After 18 h the reaction mixture is evaporated to dryness. The residue is dissolved in methylene chloride and the solution is washed with saturated NaHCO3 solution, dried and evaporated. The residue is chromatographed on silica gel using 1:1 ethyl acetate/methylene chloride as eluent to yield ethyl 8-(p-chlorophenylsulfonamido)-4-[2-(3-pyridyloxy)ethyl]-octanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153214
Source datasetuspto-grants-1992_10
ORD IDord-17d331d649a34bbba316fc6e268f8cc9
Source noteuspto-grants-1992_10