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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 731487생성일: 2026년 10월 25일

Cyclohexanone → HCID 178521584, 화합물

https://huagongshe.com/reaction/731487

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanoneHCID 7967—
반응물Sodium borohydrideHCID 4311764—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물HCID 178479277HCID 178479277—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물HCID 178521584HCID 178521584—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582769B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-b63ae0f5c959437fa391f692b89d179b
출처 메모uspto-grants-2009_09