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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740765Generated: October 30, 2026

Anthranilic Acid → HCID 21833006, compound

https://huagongshe.com/reaction/1740765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilic AcidHCID 227—
ReactantDocosanoic AcidHCID 8215—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
SolventDichloromethaneHCID 6344—
ProductHCID 21833006HCID 2183300674.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (1.58 ml) was added to a suspension of behenic acid (3.51 g) in methylene chloride (35 ml). Then, ethyl chlorocarbonate (1.08 ml) was dropwise added to the mixture while being cooled with ice. After being stirred for 1.5 hours at 0° C., the mixture, with a mixed solution of anthranilic acid (1.42 g) and triethylamine (1.44 ml) in methylene chloride (7 ml) dropwise added thereto, was stirred for 3 hour at 0° C. and for 15 hours at room temperature successively, and then cooled with ice. The reaction mixture, with triethylamine (1.58 ml) and ethyl chlorocarbonate (1.08 ml) dropwise added thereto, was stirred for 1 hour at 0° C. and for 2.5 hours at room temperature successively, and then concentrated. The residue, with chloroform added thereto, was washed with water and saturated brine successively. The organic layer was dried over sodium sulfate anhydride, and then concentrated. The residue was purified by silica gel column chromatography (silica gel 100 g, hexane-chloroform), thereby yielding 3.39 g of the aimed compound as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972929
Source datasetuspto-grants-1999_10
ORD IDord-351a2bc9b2614747a9da4652a8e2231c
Source noteuspto-grants-1999_10