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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356715Generated: October 25, 2026

Stearamidopropyl Dimethylamine → N,N-dimethyl-N-(3-methyl-4-isopropylphenyl)oxycarbonylmethyl-N-(3-(octadecanoylamino)propyl)ammonium chloride

https://huagongshe.com/reaction/1356715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStearamidopropyl DimethylamineHCID 62109—
ReactantChloroacetateHCID 518964—
Reactant3-Methyl-4-isopropylphenyl chloroacetateHCID 12084261—
SolventChloroformHCID 6212—
ProductN,N-dimethyl-N-(3-methyl-4-isopropylphenyl)oxycarbonylmethyl-N-(3-(octadecanoylamino)propyl)ammonium chlorideHCID 1208427878%

Reaction Conditions

Temperature25 °C

Reaction Steps

A 33.18 g (0.090 mol) portion of N-octadecanoyl-N′,N′-dimethyl-1,3-diaminopropane and 120 ml of chloroform were put into a flask, and 22.44 g (0.099 mol) of 3-methyl-4-isopropylphenyl chloroacetate was added thereto at 25° C. spending 5 minutes. The reaction mixture was stirred at 25° C. for 36 hours and then, after confirming disappearance of the most part of chloroacetate by 1H-NMR, the solvent was evaporated under a reduced pressure. The thus obtained viscous oil was dissolved in 300 ml of acetone and cooled to 5 to 10° C. to effect precipitation of a white precipitate. Thereafter, in the same manner as described in Inventive Example 1, the title compound (to be referred to as betaine ester (12) hereinafter) was obtained as a white solid. Yield 41.80 g (0.070 mol; yield 78.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586639B2
Source datasetuspto-grants-2003_07
ORD IDord-81a148505a4a46de9107ab02cf80836c
Source noteuspto-grants-2003_07