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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19616Generated: October 25, 2026

P-Phenylenediamine → [4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/19616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-PhenylenediamineHCID 7814—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acidHCID 853605—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product[4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl esterHCID 6731918955%

Reaction Steps

To a solution of 4-(tert-butoxycarbonylamino-methyl)-benzoic acid (1.005 g) and N-hydroxy-benzotriazole (HOBt)(0.642 g) in DMF (30 ml) are added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC)(2.76 g) and triethylamine (2.005 ml). The mixture is stirred for 1 h at ambient temperature. This solution is added at 0° C. slowly to a solution of 1,4-diaminobenzene (0.43 g) and triethylamine (0.45 ml) in DMF (5 ml). After completion of the chemical reaction the mixture is evaporated at high vacuum and the residue is partitioned between ethyl acetate and an aqueous saturated sodium bicarbonate solution. The organic phase is dried over sodium sulfate and the crude product is purified by silica gel flash chromatography. A colorless solid (0.735 g) is obtained in 55% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745446B2
Source datasetuspto-grants-2010_06
ORD IDord-8d3603ac7c024e62b278797a849ef08e
Source noteuspto-grants-2010_06