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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761884Generated: October 28, 2026

1-[4-(Benzyloxy)benzene-1-sulfonyl]-5-ethoxypyrrolidin-2-one → 5-Ethoxy-1-(4-hydroxybenzene-1-sulfonyl)pyrrolidin-2-one

https://huagongshe.com/reaction/1761884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[4-(Benzyloxy)benzene-1-sulfonyl]-5-ethoxypyrrolidin-2-oneHCID 3086695—
SolventEthanolHCID 702—
Product5-Ethoxy-1-(4-hydroxybenzene-1-sulfonyl)pyrrolidin-2-oneHCID 308672652.2%

Reaction Steps

At 20° C., and under 1000 mbar, 6.3 g of 1-(4-benzyloxyphenylsulphonyl)-5-ethoxypyrrolidin-2-one is hydrogenated in the presence of 1.2 g of catalyst (Pd at 10%), in 150 cm3 of 96° ethanol. After filtering, concentrating the filtrate, and crystallizing the residue from 96° ethanol, 2.5 g of the expected product is obtained, m.p. 162°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04829079
Source datasetuspto-grants-1989_05
ORD IDord-7a1a95b134e6494384c272eb6ed9b158
Source noteuspto-grants-1989_05