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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532642Generated: November 1, 2026

Palmitoyl chloride → HCID 9801871, compound

https://huagongshe.com/reaction/1532642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPalmitoyl chlorideHCID 8206—
ReactantTriethylamineHCID 8471—
ReactantN~1~-[3-(Dimethylamino)propyl]benzene-1,2-diamineHCID 14174121—
SolventChloroformHCID 6212—
ProductHCID 9801871HCID 9801871—

Reaction Steps

Triethylamine (0.80 ml) was added to a solution containing N-[3-(dimethylamino)propyl]-1,2-benzenediamine (1.00 g) in chloroform (10 ml) and then palmitoyl chloride (1.58 ml) was added thereto while being cooled with ice. After being stirred for 2.5 hours at room temperature, the reaction mixture was diluted with chloroform, washed with saturated sodium bydrogencarbonate aqueous solution and water successively, dried over sodium sulfate anhydride, and concentrated. Concentrated hydrochloric acid (4.3 ml) was added to a solution containing the residue (2.25 g) in ethanol (23 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 (2.21 g) was purified by silica gel column chromatography (silica gel 50 g, chloroform:methanol=30:1), thereby yielding the entitled compound (1.44 g) as yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204264B1
Source datasetuspto-grants-2001_03
ORD IDord-02ecb690294f4f02a09c1da0b44133b9
Source noteuspto-grants-2001_03