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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272563Generated: November 1, 2026

Water → Methyl 5-(benzyl(4-cyanophenyl)amino)-3-methyl-5-oxopentanoate

https://huagongshe.com/reaction/2272563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 5-(4-cyanophenylamino)-3-methyl-5-oxopentanoateHCID 86729724—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-(benzyl(4-cyanophenyl)amino)-3-methyl-5-oxopentanoateHCID 8672972526.3%

Reaction Steps

To a solution of the compound obtained in Step 1 (228 mg, 0.88 mmol) in DMF (6 mL) was added sodium hydride (60% in oil, 126 mg, 2.63 mmol) at 0° C. The reaction mixture was stirred at room temperature for 30 min, and benzyl bromide (0.156 mL, 1.31 mmol) was added thereto at 0° C. The reaction mixture was stirred at room temperature for 14 hr, to the reaction solution was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 5 to 85% ethyl acetate/hexane) to give methyl 5-(benzyl(4-cyanophenyl)amino)-3-methyl-5-oxopentanoate (81 mg, 0.230 mmol, 26.3%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120776B2
Source datasetuspto-grants-2015_09
ORD IDord-cc8b7c69b4c24364ab9150c3f12c0d7f
Source noteuspto-grants-2015_09