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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170458Generated: October 29, 2026

Sodium Carbonate → Tert-butyl 2-chloro-4-(prop-1-en-2-yl)benzoate

https://huagongshe.com/reaction/2170458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
Reactanttert-Butyl 4-bromo-2-chlorobenzoateHCID 26967600—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 2-chloro-4-(prop-1-en-2-yl)benzoateHCID 8958091492.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of tert-butyl 4-bromo-2-chlorobenzoate (1.0 g, 3.43 mmol) and 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (588 mg, 3.50 mmol) in 1,4-dioxane (40 mL) and water (10 mL) were added sodium carbonate (742 mg, 7.0 mmol) and tetrakis(triphenylphosphine)palladium (40 mg, 0.035 mmol). The resultant reaction mixture was stirred at 90° C. overnight under nitrogen atmosphere. After being cooled to room temperature, the reaction mixture was concentrated. The residue was purified by pre-HPLC to get tert-butyl 2-chloro-4-(prop-1-en-2-yl)benzoate (800 mg, 92.3%) as a yellow oil. LRMS (M+H+) m/z: calcd 253.09. found 253.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051269B2
Source datasetuspto-grants-2015_06
ORD IDord-2c513aa3254643a0a585c5fc1b9a2106
Source noteuspto-grants-2015_06