Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744887Generated: November 1, 2026

Ethyl bromoacetate → HCID 16004911, compound

https://huagongshe.com/reaction/1744887

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 mixture 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 numberUS07019024B2
Source datasetuspto-grants-2006_03
ORD IDord-1ff3ecd1c02c417fa535738bc4a32297
Source noteuspto-grants-2006_03