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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418194Generated: November 3, 2026

Ammonia → HCID 19348480, compound

https://huagongshe.com/reaction/1418194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
Reactant4-Tert-butyl-3-nitrobenzoic acidHCID 738813—
SolventAcetonitrileHCID 6342—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 19348480HCID 1934848085%

Reaction Steps

12.0 g (74.0 mmol) of N,N'-carbonyldiimidazole were added to a suspension of 15.03 g (67.3 mmol) of 4-t-butyl-3-nitrobenzoic acid in 150 ml of acetonitrile, and the resulting mixture was stirred for 1 hour, after which 20 ml (0.31 mol) of aqueous ammonia were added. The reaction mixture was stirred for 30 minutes, after which it was concentrated by evaporation under reduced pressure, and the concentrate was dissolved in ethyl acetate. The organic phase was washed with water, with 2N aqueous hydrochloric acid, with water, with a saturated aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through 150 g of silica gel, using a gradient elution method, with mixtures of ethyl acetate and hexane ranging from 1:1 to 2:1 by volume as the eluent, to give 12.68 g (yield 85%) of the title compound as crystals, melting at 114°-115° C. (from ethyl acetate-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880147
Source datasetuspto-grants-1999_03
ORD IDord-ea541de061ea4c2781ff3dee86bdf6c1
Source noteuspto-grants-1999_03