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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757398Generated: November 2, 2026

Isopropanol → HCID 23371627, compound

https://huagongshe.com/reaction/1757398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantSodium HydroxideHCID 14798—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 15290063HCID 15290063—
SolventBenzeneHCID 241—
ProductHCID 23371627HCID 23371627—

Reaction Steps

2-[1-[2-Hydroxy-2-(4-methoxyphenyl)ethyl]-1,2,5,6-tetrahydropyrid-4-yl]-4H,6H-1,3,4-thiadiazin-5-one (300 mg, 0.86 mmol) was suspended in mixed solution of isopropanol(15 ml) and benzene (25 ml), added with p-toluenesulfonic acid monohydrate (4.5 g, 0.02 mol) and refluxed for 5 hours while being dehydrated by a Dean-Stark's dehydrator. After allowing to cool to room temperature, the reaction mixture was added dropwise to 1Naqueous sodium hydroxide (30 ml). The benzen layer was separated and the water layer was further extracted three times with benzen. The benzen layer was combined with the above-mentioned benzen layer and dried over anhydrous magnesium sulfate. Benzene was removed under reduced pressure and the residue was crystallized from a little amount of ether. The solid obtained was further crystallized from ether to obtain the titled compound(145 mg) as white power.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446042
Source datasetuspto-grants-1995_08
ORD IDord-c2d2038c0f80442a981fb1d2d2ac1fdd
Source noteuspto-grants-1995_08