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HRID 731487作成日:2026年10月26日

Cyclohexanone → HCID 178521584、化合物

https://huagongshe.com/reaction/731487

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexanoneHCID 7967—
反応物Sodium borohydrideHCID 4311764—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物HCID 178479277HCID 178479277—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物HCID 178521584HCID 178521584—

反応手順

A mixture of cis-4-aminocyclohexanol hydrochloride (4 mmol) and cyclohexanone (8 mmol) and molecular sieves (3 Å, 1 g) in anhydrous MeOH (10 mL) was stirred under N2 at room temperature for 10 min. The mixture was added NaBH3CN (8 mmol) and glacial AcOH (0.1 mL) and stirred for further 24 h. Addition of NaBH4 (1.3 mmol) followed by stirring for another 10 min. The mixture was filtered and the residue was extracted with MeOH (10 mL) and the combined filtrates were evaporated to dryness. The residue was dissolved in 1 M aqueous HCl (15 mL) and washed with TBME (15 mL). The aqueous phase was added 10% aqueous NaOH until pH 14 and extracted with TBME (15 mL). The organic phase was washed with H2O (10 ml), dried (Na2SO4), and evaporated to dryness under reduced pressure affording crude cyclohexyl-cis-(4-hydroxycyclohexyl)amine 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-b63ae0f5c959437fa391f692b89d179b
出典メモuspto-grants-2009_09