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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71024Generated: October 23, 2026

Diisopropylcarbodiimide → (S)-methyl 2-[2-(4-methylphenyl)acetamido]-3-phenyl-propanoate

https://huagongshe.com/en/reaction/71024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantMethyl L-phenylalaninate hydrochlorideHCID 75736—
Reactantp-Tolylacetic acidHCID 248474—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(S)-methyl 2-[2-(4-methylphenyl)acetamido]-3-phenyl-propanoateHCID 25982542—

Reaction Steps

DMAP (194 mg, 1.58 mmol) and DIC (N,N-diisopropylcarbodiimide) (740 μl, 4.76 mmol) were added to a solution of L-phenylalanine methyl ester hydrochloride (684 mg, 3.17 mmol) and p-tolylacetic acid (500 mg, 3.33 mmol) in dry DCM (35 ml). After 24 h at room temperature the solvent was removed under reduced pressure and the crude residue was purified by flash chromatography (DCM containing 1% EtOH) to afford (S)-methyl 2-[2-(4-methylphenyl)acetamido]-3-phenyl-propanoate in quantitative yield. The product was diluted with methanol (78 ml) and then an aqueous solution of NaOH (1N, 14.2 ml, 14.2 mmol) was added. The reaction mixture was stirred for 1 h at room temperature and concentrated. Then water and HCl 1N was added until pH 2. The organic product was extracted with DCM (3×50 ml), dried with Na2CO3 and concentrated under reduced pressure to afford (S)-2-[2-(4-methylphenyl)acetamido]-3-phenyl-propionic acid as a white solid (94% c.y.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822698B2
Source datasetuspto-grants-2014_09
ORD IDord-aa88a2d6a18c477291b2a4cfc90a52d7
Source noteuspto-grants-2014_09