3785-34-0Relevant articles and documents
Studies on synthesis, characterization, micellar features, and solubilization of four novel cationic gemini surfactants
Bilgen, Sel?uk,Sarikaya, Ikbal,ünver, Yasemin,Akba?, Halide
, p. 1522 - 1532 (2021)
Four novel cationic gemini surfactants with the same hydrocarbon chain lengths but different spacers have been investigated in this article. After these cationic gemini surfactants have been synthesized, their structures have been characterized by appropr
Synthesizing method of imidazole type Gemini surfactant
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Paragraph 0010, (2016/10/09)
The invention discloses a synthesizing method of imidazole type Gemini surfactant. The synthesizing method is characterized in that N-alkyl imidazole is synthesized by using imidazole and alkyl bromide, reaction temperature is 25 DEG C, reaction time is 8 hours, and the yield is about 70%; bromoacetic acid 1, 4-butanediyl ester is synthesized by using bromoacetic acid and dihydric alcohol, reaction temperature is 125 DEG C, and reaction time is 24 hours; the final product is synthesized by using the N-alkyl imidazole and the bromoacetic acid 1, 4-butanediyl ester, reaction temperature is 85 DEG C, reaction time is 36 hours, and yield is about 85%. The synthesizing path is shown as follows, wherein n=2, 4, 6.
Bromoacetyl bromide: A versatile and selective cleaving agent for ethers and acetals
Schneider, David F.,Viljoen, Murray S.
, p. 721 - 728 (2007/10/03)
It is shown that bromoacetyl bromide can be utilized for the selective cleavage of ethers and acetals in high yields. With cyclic ethers and acetals as starting materials, cleavage products are produced with two strategically positioned bromo substituents which may be exploited for selective extention of the carbon chain.