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HRID 731488作成日:2026年10月27日

1-Bromopropane → HCID 178459264、化合物

https://huagongshe.com/reaction/731488

反応式

関与物質

役割名称HCID仕込み量
反応物1-BromopropaneHCID 7840—
反応物Sodium hydrideHCID 24758—
反応物HCID 178521584HCID 178521584—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物HCID 178459264HCID 178459264—

反応手順

A mixture of NaH (60% susp., 1.4 mmol) and ethylene glycol dimethylether (3 mL) was added cyclohexyl-cis-(4-hydroxycyclohexyl)-amine (0.36 mmol) and the mixture was stirred under N2 at rt for 5 min followed by addition of propylbromide (5.5 mmol). The mixture was refluxed for 18 h under N2. The reaction mixture was cooled to rt and quenched with anhydrous EtOH (0.5 mL). The mixture was filtered and the residue was extracted with ethylene glycol di-methylether (2 mL). The organic phase was evaporated to dryness under reduced pressure and co-evaporated with toluene (10 LI). The residue was added HCl in MeOH (1.25 M, 5 mL) and evaporated under reduced pressure affording a white solid. The solid was washed with TBME (2 mL) and dissolved in a mixture of DCM (5 mL) and 1 M aqueous NaOH (5 mL). The organic phase was washed with H2O (5 mL), dried (Na2SO4), and evaporated under reduced pressure to give the desired cyclohexyl-cis-(4-propoxycyclohexyl)amine as an oil which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582769B2
出典データセットuspto-grants-2009_09
ORD IDord-377a96409dfe44aabf92639ca45e390c
出典メモuspto-grants-2009_09