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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076338Generated: October 31, 2026

Diethyl Ether → 1-Dodecanaminium, N-(2-hydroxyethyl)-N,N-dimethyl-, bromide (1:1)

https://huagongshe.com/reaction/1076338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant2-(Dimethylamino)ethanolHCID 7902—
ReactantButyl isocyanateHCID 8110—
Reactant1-BromododecaneHCID 8919—
SolventEthyl AcetateHCID 8857—
Product1-Dodecanaminium, N-(2-hydroxyethyl)-N,N-dimethyl-, bromide (1:1)HCID 81486—
ProductHCID 5247103HCID 5247103—

Reaction Steps

2-hydroxyethyldimethyldodecylammonium bromide, N-butylcarbamate is prepared in the following manner. A solution of 58 g. (0.65 mole) 2-dimethylaminoethanol in 150 ml. ether was treated over a period of 1.5 hours with 70 g. (0.71 mole) n-butyl isocyanate. After stirring another two hours the reaction mixture was stripped of ether and distilled in vacuum. The product, 2-dimethylaminoethyl N-butylcarbamate was collected at 106°/1.2 Torr. For quaternization 75 g. (0.40 mole) of the above prepared amine was combined with 105 g (0.42 mole) 1-bromododecane and allowed to stand stoppered for nine days. At this time the reaction mixture was a stiff gel with some crystalline portions. By solution in ethyl acetate (900 ml.) and chilling, 160 g. of product was obtained in crystalline form. After two more recrystallizations from ethyl acetate, the material melted at 64°C. to liquid crystals and to a liquid at 115°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03956479
Source datasetuspto-grants-1976_05
ORD IDord-347c8da72d5c432f8a4ff1d666a6006a
Source noteuspto-grants-1976_05