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HRID 2371090作成日:2026年10月26日

Butylamine → N''-Butyl-N,N,N',N'-tetramethyl-guanidine

https://huagongshe.com/reaction/2371090

反応式

関与物質

役割名称HCID仕込み量
反応物ButylamineHCID 8007—
反応物TetramethylureaHCID 12437—
反応物Oxalyl chlorideHCID 65578—
溶媒1,1-DichloroethaneHCID 6365—
生成物N''-Butyl-N,N,N',N'-tetramethyl-guanidineHCID 525255—

反応手順

N,N,N′,N′-tetramethyl-N″-butylguanidine was prepared as follows: 9.3 g tetramethyl urea was added to 80 mL dry dichloroethane in a two-neck 250 mL round-bottom-flask. 11.3 mL oxalyl chloride was added and the solution was heated at 70*C for two hours. The solvent was evaporated in vacuo after the solution cooled to room temperature. Residual solid was then dissolved in dry acetonitrile and cooled to 0° C. 15 mL butyl amine (1.02 eq) was slowly added. The solution was slowly warmed and allowed to reflux for one hour. Finally, the mixture was cooled to room temperature and the solvent was removed in vacuo to yield 9 g of a clear oil. 1H(CDCl3): δ (ppm): 2.99 (t, 2H); 2.62 (s, 3H); 2.53 (s, 3H); 1.39 (quintet, 2H); 1.24 (quintet, 2H); 0.78 (t, 3H). The synthesis was performed several times and the yield ranged from 37%-70%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08710265B2
出典データセットuspto-grants-2014_04
ORD IDord-4404b455e0ba4d3f9cc7233c1d09ccc1
出典メモuspto-grants-2014_04