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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430815Generated: October 30, 2026

4-tert-Butylbenzoic acid → N-[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-4-tert-butyl-benzamide

https://huagongshe.com/reaction/430815

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-Butylbenzoic acidHCID 7403—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamideHCID 22255921—
SolventDimethylformamideHCID 6228—
ProductN-[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-4-tert-butyl-benzamideHCID 18352025—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 0.589 g (3.026 mmol) 4-tert-butylbenzoic acid (Aldrich, Milwaukee Wis.) 1.06 mL (6.5 mmol) N,N-diisopropylethylamine, and 1.15 g (3.026 mmol) O-Benzotriazol-1-yl-N,N,N′,N′-bis(tetramethylene)-uronium hexafluorophosphate in 6 mL dry DMF was stirred in an ice bath for 35 minutes, when 1.00 g (3.026 mmol) of 2-Amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide (Example 1, Step B) was added. The resulting solution was warmed to 25° C. and stirred for 60 minutes. The mixture was poured into 20 mL diethyl and washed sequentially with 25 mL each of saturated aqueous sodium bicarbonate solution and twice with brine. The mixture was then dried over anhydrous sodium sulfate and concentrated at reduced pressure giving a pale amber solid that was purified by column chromatography on silica gel with 30% ethyl acetate in hexane to give N-[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethyl]-4-tert-butyl-benzamide as a white solid; mp 124-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323243B1
Source datasetuspto-grants-2001_11
ORD IDord-1f2627d0a6ee4a678b8bd880b3af32f6
Source noteuspto-grants-2001_11