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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525972Generated: November 2, 2026

Salicylic Acid → N-(2-(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamidopropyl)-2-hydroxybenzamide

https://huagongshe.com/reaction/1525972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylic AcidHCID 338—
ReactantImidazoleHCID 795—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 59193269HCID 59193269—
SolventEthyl AcetateHCID 8857—
ProductN-(2-(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamidopropyl)-2-hydroxybenzamideHCID 5919332350.5%

Reaction Steps

To a solution of (4Z,7Z,10Z,13Z,16Z,19Z)—N-(1-aminopropan-2-yl)docosa-4,7,10,13,16,19-hexaenamide (1.60 g, 4.2 mmol), 2-hydroxybenzoic acid (0.57 g, 4.2 mmol) and imidazole (0.29 g, 4.2 mmol) in EtOAc (40 mL) at 0° C. was added a solution of DCC (0.87 g, 4.2 mmol) in EtOAc (40 mL). The mixture was allowed to warm to RT, stirred (16 h) and filtered. The solvent was removed under reduced pressure and the crude product was purified by chromatography on silica gel, eluting with EtOAc-PE (0-50%) to afford N-(2-(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamidopropyl)-2-hydroxybenzamide (1.07 g, 50.5%) as a light yellow oil. Mass calculated for C32H44N2O3=504.70; found: [M+H]+=505.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085527B2
Source datasetuspto-grants-2015_07
ORD IDord-ad0fde4c075049cdabd323ac81d51f71
Source noteuspto-grants-2015_07