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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532653Generated: October 30, 2026

Stearoyl chloride → HCID 15518372, compound

https://huagongshe.com/reaction/1532653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStearoyl chlorideHCID 8212—
ReactantTriethylamineHCID 8471—
ReactantHCID 22013772HCID 22013772—
SolventChloroformHCID 6212—
ProductHCID 15518372HCID 1551837282.7%

Reaction Steps

Triethylamine (0.42 ml) was added to a solution containing N-(3-morpholinopropyl)-1,2-benzenediamine (0.640 g) in chloroform (3.5 ml), and then a solution containing stearoyl chloride (0.825 g) in chloroform (3.5 ml) was added thereto while being cooled with ice. After being stirred for 3 hours at room temperature, the reaction mixture was diluted with chloroform, washed with saturated sodium hydrogencarbonate aqueous solution and water successively, dried over sodium sulfate anhydride, and concentrated. Concentrated hydrochloric acid (2.25 ml) was added to a solution containing the residue (1.442 g) in ethanol (15 ml). After being stirred for 1.5 hours at 90° C., the reaction mixture was concentrated. The residue, with ethyl acetate added thereto, was washed with 1N sodium hydroxide aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. The residue (1.296 g) was purified by silica gel column chromatography (silica gel 40 g, ethyl acetate), thereby yielding the entitled compound (1.088 g) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204264B1
Source datasetuspto-grants-2001_03
ORD IDord-41a2988dd10f4466b3b8c94a71790ff5
Source noteuspto-grants-2001_03