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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745221생성일: 2026년 10월 26일

Potassium Carbonate → Benzenemethanol, 4-chloro-alpha-ethyl-alpha-(4-((6-methyl-2-pyridinyl)methoxy)phenyl)-

https://huagongshe.com/reaction/745221

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-(Chloromethyl)-6-methylpyridineHCID 76546—
반응물alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매Ethyl AcetateHCID 8857—
생성물Benzenemethanol, 4-chloro-alpha-ethyl-alpha-(4-((6-methyl-2-pyridinyl)methoxy)phenyl)-HCID 3022025—

반응 단계

13.1 g. of α-ethyl-α-(4-chlorophenyl)-4-hydroxybenzyl-alcohol, 14 g. of anhydrous potassium carbonate, 0.85 g. of tetrabutylammonium hydrogensulfate and 7.8 g. of 2-methyl-6-chloromethyl-pyridine in 140 ml. of ethyl acetate are boiled for 18 hours. The solvent is distilled off under reduced pressure, to the residue water is added, and it is extracted with ether. The ethereal solution is washed to neutral with a 5% aqueous potassium hydroxide solution and subsequently water, dried over anhydrous magnesium sulfate, and evaporated in vacuo. Crystallization of the residue from a mixture of hexane and ethyl acetate yields 13.6 g. of the title compound, melting at 100° to 101° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04598080
출처 데이터셋uspto-grants-1986_07
ORD IDord-2be7deb7c5794779bbdbc1444ceead4d
출처 메모uspto-grants-1986_07