돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 373366생성일: 2026년 10월 24일

2-Cyclohexen-1-one → 3-Butylcyclohexanone

https://huagongshe.com/ko/reaction/373366

반응식

참여 물질

역할이름HCID투입량
반응물2-Cyclohexen-1-oneHCID 13594—
반응물HCID 178418265HCID 178418265—
용매TetrahydrofuranHCID 8028—
생성물3-ButylcyclohexanoneHCID 56619394%

반응 조건

온도-78 °C

반응 단계

A THF (5 mL) suspension of CuBr.Me2S (26.3 mg, 0.128 mmol) was treated with 1.0 equiv of n-BuLi at -78° C. under an argon atmosphere. The mixture was allowed to warm up slightly with the formation of a bright yellow solid. The mixture was again cooled to -78° C. and treated with Li(CHIRAMT) formed from compound 4 (85.8 mg, 0.261 mmol) and n-BuLi (1.0 equiv). The yellow slurry was stirred with gradual warming until a homogeneous burgundy solution was obtained. In the case of R=Me, a homogeneous mixture was not obtained even after prolonged stirring at room temperature, and it was evident that unreacted (CuMe)n was still present. The solution was cooled to -78° C. and THF (8 mL each) solutions of n-BuMgCl (25.0 equiv) and cyclohexenone (0.3068 g, 3.19 mmol) were added dropwise and simultaneously over a 5 min period. The resulting reaction mixture was stirred for an additional 10 min at -78° C., quenched with saturated aqueous NH4Cl solution (7 mL), and worked up as described in the previous section. Pure 3-butylcyclohexanone (0.4617 g, 94%) was obtained as checked by glc.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05162586
출처 데이터셋uspto-grants-1992_11
ORD IDord-5305ffc08cde4e59b1a355accdbad04c
출처 메모uspto-grants-1992_11