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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64425Generated: October 25, 2026

Hydrochloric Acid → Tert-butyl 3-(2-formyl-3-methylphenyl)propanoate

https://huagongshe.com/reaction/64425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantTert-butyl 3-[2-(hydroxymethyl)-3-methylphenyl]propanoateHCID 86713433—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 3-(2-formyl-3-methylphenyl)propanoateHCID 8671343592.6%

Reaction Steps

To a solution of 770 mg of tert-butyl 3-[2-(hydroxymethyl)-3-methylphenyl]propanoate in 16 ml of dimethylsulfoxide were added 4 ml of triethylamine and 1.22 g of a sulfur trioxide pyridine complex, followed by stirring at room temperature for 5 hours. To the reaction mixture were added diluted hydrochloric acid and ethyl acetate to carry out a layer separation operation. The organic layer was sequentially washed with water, saturated aqueous sodium hydrogen carbonate solution, water, and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 707 mg of tert-butyl 3-(2-formyl-3-methylphenyl)propanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447090B2
Source datasetuspto-grants-2016_09
ORD IDord-bb620d24890d4ac992089582cc8b1162
Source noteuspto-grants-2016_09