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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635911Generated: October 30, 2026

Ethyl bromoacetate → HCID 16004911, compound

https://huagongshe.com/reaction/635911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant3,3-DiphenylpropylamineHCID 79698—
SolventAcetonitrileHCID 6342—
ProductHCID 16004911HCID 1600491169.1%

Reaction Steps

2.132 g (10.1 mmol) 3,3-diphenylpropylamine (Aldrich, Milwaukee, Wis.) was added to a mixture of 0.853 g (5.11 mmol) ethyl bromoacetate (Aldrich) and 2.7 g (19.57 mmol) potassium carbonate in 14 ml acetonitrile at rom temperature. The mixture was stirred under argon for 18 hours. The reaction mire was filtered, the solvent evaporated and the residue chromatographed on a silica gel column with 40% ethyl acetate in hexanes to give 1.05 g (yield 69%) N-[(3,3-diphenyl)propyl]glycine ethyl ester (Compound A22) as an oil. NMR spectra of the product showed: 1H NMR (CDCl3, 300 MHz) 7.40-7.10 (m, 10 H), 4.14 (q, 2 H),4.03 (t, 1 H),3.33 (s, 2 H), 2.56 (t, 2 H), 2.24 (dt, 2 H), 1.22 (t, 3 H); 13C NMR (CDCl3, 75 MHz) 172.44, 144.66, 128.43, 127.75, 126.15, 60.63, 50.93, 48.80, 47.92, 35.85, 14.17. 0.019 g of A28 was also isolated from the silica gel column.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191165B1
Source datasetuspto-grants-2001_02
ORD IDord-6bd69beeabde437a9e102b44226d9c61
Source noteuspto-grants-2001_02