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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465914Generated: October 31, 2026

p-Toluenesulfonic acid → N-(2-hydroxy-3-n-propyl-4-methoxybenzoyl)thiazolidine

https://huagongshe.com/reaction/465914

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantN-(2-methoxymethoxy-3-n-propyl-4-methoxybenzoyl)thiazolidineHCID 14719505—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN-(2-hydroxy-3-n-propyl-4-methoxybenzoyl)thiazolidineHCID 1471950693.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

The N-(2-methoxymethoxy-3-n-propyl-4-methoxybenzoyl)thiazolidine (9.0 g) was dissolved in a solution of methanol (100 ml)-water (20 ml). To the solution was added p-toluenesulfonic acid (2 spoonfuls in spatula) and the mixture was agitated at 60° C. for 23 hours. The reaction mixture was concentrated in evacuated atomosphere to about one fourth of the original volume. Saturated aqueous solution of sodium bicarbonate was added to the concentrate, and the mixture was extracted twice with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and concentrated in evacuated atomosphere. The residue was subjected to column chromatography using silica gel, and there was obtained N-(2-hydroxy-3-n-propyl-4-methoxybenzoyl)thiazolidine (7.3 g) from fractions eluted with n-hexane-ethyl acetate (5:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155106
Source datasetuspto-grants-1992_10
ORD IDord-47637f04ae004b55b5939e8662ce861e
Source noteuspto-grants-1992_10