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HRID 378016作成日:2026年10月25日

N-(Octan-2-yl)acetamide → 1-Heptanamine, 1-methyl, N-ethyl

https://huagongshe.com/reaction/378016

反応式

関与物質

役割名称HCID仕込み量
反応物N-(Octan-2-yl)acetamideHCID 529463—
反応物(Dimethyl sulfide)trihydroboronHCID 12423031—
溶媒TetrahydrofuranHCID 8028—
生成物1-Heptanamine, 1-methyl, N-ethylHCID 52505378.4%

反応手順

A 2M THF solution of borane-dimethylsulfide (31.5 mL, 63 mmol) was added dropwise to an ice water-cooled solution of N-(1-methylhept-1-yl)acetamide (5.13 g, 30 mmol) in THF (60 mL). The resulting solution was stirred at RT for 1 h, then was refluxed overnight. With ice-water cooling, the excess borane-dimethylsulfide was quenched by the dropwise addition of methanol (10 mL), and the mixture was allowed to stand at RT overnight. The amine hydrochloride could not be precipitated with the addition of HCl gas, so the amine hydrochloride was extracted into dilute HCl. The acidic aq solution was extracted with ether, then made basic and extracted with ethyl acetate. The ethyl acetate solution was dried (MgSO4) and concentrated to afford 3.70 g of impure N-ethyl-N-(1-methylhept-1-yl)amine as an amber oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06028101
出典データセットuspto-grants-2000_02
ORD IDord-8892415746e64ac283e12826e1626158
出典メモuspto-grants-2000_02