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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675253Generated: October 30, 2026

Ethyl Acetate → Methyl 4-tert-butyl-3-(prop-1-en-2-yl)benzoate

https://huagongshe.com/reaction/1675253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
ReactantMethyl 3-bromo-4-(tert-butyl)benzoateHCID 11959028—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 4-tert-butyl-3-(prop-1-en-2-yl)benzoateHCID 5930065388%

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 3-bromo-4-tert-butylbenzoate (500 mg, 1.80 mmol, prepared according to the procedure of Hambley T. W. et al. Aust. J. Chem., 1990, 43, 807-814) and commercially available isopropenylboronic acid pinacol ester (0.693 mL, 3.6 mmol) were suspended in toluene (7 mL). Potassium carbonate (765 mg, 5.5 mmol) was added followed by Pd(PPh3)4 (213 mg, 0.180 mmol). The resulting mixture was heated to 100° C. and stirred for 24 hours. After cooling to room temperature, the mixture was treated with EtOAc (5 mL) and brine (5 mL). The organic layer was separated, washed twice with brine, dried with MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (0-10% EtOAc/hexane) to give 26.2 (378 mg, 88%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003648B2
Source datasetuspto-grants-2011_08
ORD IDord-ef27c8ded03542fa8bbc083f3ee10957
Source noteuspto-grants-2011_08