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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494155Generated: November 1, 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/1494155

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-chloro- phenylsulfonyl)-N-(t-butoxycarbonyl)amino]-4-[2-(3-pyridyl- oxy)-ethyl]octanoate in 30 ml trifluoroacetic acid is stirred at room temperature. After 18 hours 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 numberUS05025025
Source datasetuspto-grants-1991_06
ORD IDord-fd6ff43dba7d4972b3e7ea5bde113f5e
Source noteuspto-grants-1991_06