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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454513Generated: October 29, 2026

Sodium Carbonate → Tert-butyl 4-(3-(tert-butoxycarbonylamino)phenyl)-2-nitrobenzoate

https://huagongshe.com/reaction/454513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium BicarbonateHCID 516892—
Reactant(3-Boc-aminophenyl)boronic acidHCID 2773228—
Reactanttert-Butyl 4-bromo-2-nitrobenzoateHCID 26369829—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(3-(tert-butoxycarbonylamino)phenyl)-2-nitrobenzoateHCID 6699003682.6%

Reaction Steps

Water (0.6 mL), sodium carbonate (0.16 g), 3-(tert-butoxycarbonylamino)phenylboronic acid (0.14 g), and tetrakis(triphenylphosphine)palladium(0) (29 mg) were added to an ethylene glycol dimethyl ether (2.0 mL) solution of tert-butyl 4-bromo-2-nitrobenzoate (0.15 g), followed by heating to reflux under a nitrogen atmosphere for 2 hours. The reaction mixture was cooled to room temperature, and then ethyl acetate and a saturated aqueous solution of sodium bicarbonate were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 95-91% hexane/ethyl acetate] to obtain 0.17 g of tert-butyl 4-(3-(tert-butoxycarbonylamino)phenyl)-2-nitrobenzoate as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-b7f6c180e2d945b98937b14d94f7d28c
Source noteuspto-grants-2013_07