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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719712Generated: October 26, 2026

Water → HCID 20266437, compound

https://huagongshe.com/reaction/1719712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium borohydrideHCID 4311764—
Reactant2-[2-(Pyridin-4-yl)ethyl]-1lambda~6~,2-thiazolidine-1,1-dioneHCID 20266434—
SolventEthanolHCID 702—
ProductHCID 20266437HCID 20266437—

Reaction Steps

Benzyl bromide (3.1 cm3) was added at room temperature to a stirred solution of 2-[2-(4-pyridyl)ethyl]isothiazolidine-1,1-dioxide (4.9 g) in ethanol (30 cm3) and the mixture was heated under reflux for 3 hours. After cooling to room temperature, water (30 cm3) was added followed by sodium borohydride (1.2 g) and the mixture was stirred for 1 hour. Volatile material was removed in vacuo and the residue was treated with 2M hydrochloric acid to pH1, followed by neutralisation with sodium carbonate solution and subsequent extraction with chloroform (3×100 cm3). The dried (MgSO4) chloroform extract was evaporated to give an oil which was chromatographed on silica ("Merck" 60.9385) eluting with methanol:chloroform, 1:49, to give 2-[2-(1-benzyl-1,2,3,6-tetrahydropyrid-4-yl)ethyl]isothiazolidine-1,1-dioxide as an oil (4.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542132
Source datasetuspto-grants-1985_09
ORD IDord-4152b37aecf44aac816bee5d5de1703a
Source noteuspto-grants-1985_09