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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110238Generated: November 3, 2026

Sodium Hydroxide → HCID 19018986, compound

https://huagongshe.com/reaction/1110238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 19018968HCID 19018968—
ReactantHCID 19389138HCID 19389138—
SolventMethanolHCID 887—
ProductHCID 19018986HCID 19018986—

Reaction Steps

A mixture of 1.0 g (3.45 mmol) of 4-tetradecylphenyl aniline (Aldrich Chemical Company), 5.0 ml (0.052 mol) of methyl bromoacetate, 0.95 g (6.9 mmol) of potassium carbonate and 0.5 g (3.45 mmol) of sodium iodide in 15 ml of DMF was stirred and heated at 100° for 45 hours. The solvent was removed at reduced pressure and water was added to the residue. The product was extracted with ethyl acetate and the extract was washed with sodium bisulfite solution, dried and concentrated. The residue was purified by chromatography on silica gel using 25% ethyl acetate-hexane to give 0.7 g of N-(2-methoxy-2-oxoethyl)-N-(4-tetradecylphenyl)glycine methyl ester. This dimethyl ester was hydrolyzed by treatment with 1.5 ml of 6N NaOH in 50 ml of methanol. The mixture was warmed briefly to dissolve the ester and then was kept at room temperature for 3 days. The solvent was removed at reduced pressure and the residue was acidified to pH 2. The product was extracted with ethyl acetate and the dried extract was concentrated at reduced pressure to a solid which was recrystallized from methanol-water to give 0.26 g, mp 160°-165°, of N-(carboxymethyl)-N-(4-tetradecylphenyl)glycine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324747
Source datasetuspto-grants-1994_06
ORD IDord-b307cd71c2954d48b20e2a58d89fad63
Source noteuspto-grants-1994_06