HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090725Generated: November 1, 2026
Dimethylamine → dodecyl-N,N-dimethylaminoacetate
https://huagongshe.com/reaction/1090725
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Dodecyl chloroacetate | HCID 228182 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | dodecyl-N,N-dimethylaminoacetate | HCID 129378 | 100% |
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, 0.1M 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05082866 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-1f3e971581e3411fb577b6147559207b |
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| Source note | uspto-grants-1992_01 |
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