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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408848Generated: November 2, 2026

Ethyl 3,4-Diaminobenzoate → 4-Methoxycarbonylphenylboronic acid

https://huagongshe.com/reaction/1408848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3,4-DiaminobenzoateHCID 458855—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product4-Methoxycarbonylphenylboronic acidHCID 2734369228.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

Referring to Scheme 11-1, to a solution of the bromide 1 (2.0 g, 4.2 mmol, prepared according to published conditions) in dioxane (60 mL) was added bis(pinacolato)diboron (4.32 g, 17 mmol), Pd(PPh3)4 (0.49 g, 0.42 mmol) and potassium acetate (2.06 g, 21 mmol) under nitrogen atmosphere. The reaction mixture was stirred at 80° C. for 5 h, and then diluted with ethyl acetate (150 mL). The organic phase was washed with H2O (20 mL), dried over sodium sulfate and concentrated in vacuo. The residue was further purified by silica gel column chromatography (hexanes/ethyl acetate=1/4 to 0/1 (v/v)) to give 2 (1.73 g, 79% yield). LC-MS (ESI): m/z 523.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921369B2
Source datasetuspto-grants-2014_12
ORD IDord-b1256e96338b43389542ce5345398994
Source noteuspto-grants-2014_12