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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132104생성일: 2026년 10월 26일

Cyclohexanone → 1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanol

https://huagongshe.com/reaction/132104

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanoneHCID 7967—
반응물PentaneHCID 8003—
반응물1-Bromo-3-tert-butylbenzeneHCID 343798—
반응물HCID 178418306HCID 178418306—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매Ammonium ChlorideHCID 25517—
생성물1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanolHCID 5973374381%

반응 단계

A solution of 1.7 M tert-butyllithium in pentane (32.0 mL, 54.4 mmol) was added to a solution of 1-bromo-3-tert-butyl-benzene (5.54 g, 26.0 mmol) in tetrahydrofuran (60 mL) at −78° C. After stirring for 1 h, cyclohexanone (2.00 g, 18.2 mmol) in tetrahydrofuran (15 mL) was added. After stirring for 18 h, during which time the solution warmed to ambient temperature, the solution was diluted with saturated aqueous ammonium chloride and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was flash chromatographed with 49:1, 24:1, 23:2 hexanes:ethyl acetate as the eluant to yield 3.61 g (81% yield) of 1-(3-tert-butyl-phenyl)-4-methylene-cyclohexanol as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07385085B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-f0668dfcdcd04782a255a587cf61429e
출처 메모uspto-grants-2008_06