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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374676Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 22418852, compound

https://huagongshe.com/reaction/374676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 22418825HCID 22418825—
SolventPyridineHCID 1049—
ProductHCID 22418852HCID 2241885270.9%

Reaction Steps

238 mg of tert-butyl 2-(2,3-ethylenedioxybenzyl)-3-hydroxypropionate was dissolved in 4 ml of dry pyridine, and 170 mg of p-toluenesulfonyl chloride was added thereto. The mixture was reacted at room temperature overnight and then concentrated under reduced pressure. The residue was dissolved in 50 ml of ethyl acetate and washed sequentially with 50 ml of a 5% potassium hydrogensulfate aqueous solution, with 50 ml of a 4% sodium hydrogencarbonate aqueous solution and with 50 ml of a saturated sodium chloride aqueous solution. The organic layer was dried over anhydrous magnesium sulfate, then concentrated under reduced pressure and purified by silica gel column chromatography (n-hexane/ethyl acetate=3/1) to obtain 257 mg of tert-butyl 2-(2,3-ethylenedioxybenzyl)-3-p-toluenesulfonyloxypropionate as colorless transparent syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05481036
Source datasetuspto-grants-1996_01
ORD IDord-616113c51524430b9fa660075d160c16
Source noteuspto-grants-1996_01