Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633955Generated: October 31, 2026

Sodium Chloride → 3-{4-[(4-Tert-butylphenylamino)methyl]benzoylamino}propionic acid methyl ester

https://huagongshe.com/reaction/1633955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantEthyl orthoformateHCID 31214—
Reactant4-Tert-ButylanilineHCID 69861—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(4-Formylbenzoylamino)propionic acid methyl esterHCID 16100325—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
Product3-{4-[(4-Tert-butylphenylamino)methyl]benzoylamino}propionic acid methyl esterHCID 1610034130%

Reaction Steps

The above 3-(4-formylbenzoylamino)propionic acid methyl ester (2.0 g, 8.5 mmol) was dissolved in DMF (20 mL). Triethyl orthoformate (10 mL), glacial acetic acid (1 mL), sodium cyanoborohydride (0.81 g, 12.8 mmol) and 4-tert-butylaniline 1.27 g, 8.5 mmol) were added and the resulting mixture was stirred at room temperature for 16 hours. The mixture was added saturated aqueous sodium chloride (100 mL) and the mixture was extracted with ethyl acetate (3×100 mL). The combined organic extracts were washed with saturated aqueous sodium chloride (3×100 mL). The organic phase was dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with a mixture of ethyl acetate and heptane (1:1) to afford 0.87 g (30%) of 3-{4-[(4-tert-butylphenylamino)methyl]benzoylamino}propionic acid methyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-476916ddc9e54c038baab9b6c2ce9b1a
Source noteuspto-grants-2003_01