Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437380Generated: November 2, 2026

3-Amino-5-nitrobenzoic acid → 3-Nitro-5-(3,6,9-trioxadecanamido)benzoic acid

https://huagongshe.com/reaction/437380

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-5-nitrobenzoic acidHCID 239342—
Reactant2-[2-(2-Methoxyethoxy)ethoxy]acetyl chlorideHCID 2759571—
Solvent1,4-DioxaneHCID 31275—
Product3-Nitro-5-(3,6,9-trioxadecanamido)benzoic acidHCID 70623675—

Reaction Steps

A mixture of 14.6 g. of 3-amino-5-nitrobenzoic acid and 17.1 g. of 3,6,9-trioxadecanoic acid chloride in 200 ml. of dioxane was heated at reflux for 24 hours. The reaction mixture was concentrated to remove the solvent. The residue was dissolved in dilute sodium hyroxide and then acidifed with hydrochloric acid. The resulting product (13.6 g., m.p. 130° C.) was recrystallized from acetonitrile to give 3-nitro-5-(3,6,9-trioxadecanamido)benzoic acid as a beige solid, m.p. 136°-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031088
Source datasetuspto-grants-1977_06
ORD IDord-e57ff0299f1b4efca11fa7ead4f25958
Source noteuspto-grants-1977_06