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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111424Generated: November 4, 2026

Dimethylamine → dodecyl-N,N-dimethylaminoacetate

https://huagongshe.com/reaction/1111424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantAcetic acid, 2-chloro-, dodecyl esterHCID 228182—
SolventDiethyl EtherHCID 3283—
Productdodecyl-N,N-dimethylaminoacetateHCID 129378100%

Reaction Steps

Dodecyl chloroacetate (5.5 g, 0.021 mol) was dissolved in 20 ml of ether and the resultant solution was cooled in an ice-bath. Dimethylamine (40 ml, 0.1 M in ether) was added to the cooled solution of dodecyl chloroacetate. The reaction mixture was stirred at room temperature for two hours, then filtered through a filter paper to remove the white solid which formed. The filtrate was concentrated to give a liquid product which was chromatographed through a column of silica gel (60-200 mesh) using ethyl acetate as the eluent. The purity of the fractions was checked by thin layer chromatography. The pure fractions were combined and the solvent was removed by a rotary evaporator under reduced pressure to afford 5.8 g (100% yield) of dodecyl (N,N-dimethylamino)acetate. 1HNMR(CCl4) δ0.83(3H, t, CH3); 1.20[20 H, s, broad, --(CH2)10 ]; 2.23[6H, s, (CH3)2N--]; 3.0 (2H, s, --CH2 --N); 3.93 (2H, t, J=6 Hz, --OCH2 --) νmax (film): 2940,2870,2790 (CH); 1760, 1740(C=O); 1200, 1170 (--C--O--C) cm-1. m/e 271; C16H33NO2 requires 271.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980378
Source datasetuspto-grants-1990_12
ORD IDord-1bc7a971e61c496a99a46c42a1baf260
Source noteuspto-grants-1990_12