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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532673Generated: October 30, 2026

Stearoyl chloride → HCID 9890245, compound

https://huagongshe.com/reaction/1532673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStearoyl chlorideHCID 8212—
ReactantTriethylamineHCID 8471—
ReactantHCID 43168878HCID 43168878—
SolventDichloromethaneHCID 6344—
ProductHCID 9890245HCID 989024531.3%

Reaction Steps

Triethylamine (0.557 g) was added to a solution containing N1-[3-(dimethylamino)propyl]4-methyl-1,2-benzenediamine (1.037 g) in dichloromethane (5 ml), and then a solution containing stearoyl chloride (1.515 g) in dichloromethane (5 mnl) was added thereto while being cooled with ice. After being stirred for 4.5 hours at room temperature, the reaction mixture was diluted with dichloromethane, washed with saturated sodium hydrogencarbonate aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. Concentrated hydrochloric acid (3.5 ml) was added to a solution containing the residue (1.97 g) in ethanol (20 ml). After being stiffed for 5.5 hours at 90° C., the reaction mixture was concentrated. The residue, with chloroform added thereto, was washed with 0.5N sodium hydroxide aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. The residue (1.03 g) was purified by silica gel column chromatography (silica gel 30 g, chloroform:methanol=50:1-1:1), thereby yielding the entitled compound (0.714 g) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204264B1
Source datasetuspto-grants-2001_03
ORD IDord-c2f542b22a724a3a8c965b7d636f0dd3
Source noteuspto-grants-2001_03