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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 461717생성일: 2026년 10월 25일

Tetrahydrofuran → alpha-Hydroxy-p-tolyl 2-thienyl ketone

https://huagongshe.com/reaction/461717

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Ammonium ChlorideHCID 25517—
반응물2-ThiophenecarbonitrileHCID 66087—
반응물2-[(4-Bromophenyl)methoxy]oxaneHCID 598168—
반응물MagnesiumHCID 5462224—
생성물alpha-Hydroxy-p-tolyl 2-thienyl ketoneHCID 21391792—

반응 단계

To a stirred and refluxing Grignard-complex, previously prepared starting from 7.2 parts of magnesium and 81.4 parts of 2-(p-bromobenzyloxy)tetrahydropyran in 200 parts of dry tetrahydrofuran, is added dropwise a solution of 32.7 parts of 2-thiophenecarbonitrile in 70 parts of dry tetrahydrofuran (exothermic reaction: reflux temperature is maintained). Upon completion, stirring at reflux is continued for 4 hours. The reaction mixture is cooled and decomposed with 150 parts of a saturated ammonium chloride solution at about 15° C. The whole is poured onto water and the product is extracted with ether. The organic layer is washed four times with water, dried, filtered and acidified with gaseous hydrogen chloride: an oil is separated. The ether is decanted and the oily product is dissolved in 300 parts of water and 150 parts of concentrated hydrochloric acid solution. The solution is stirred with activated charcoal, filtered and the filtrate is stirred and refluxed for 10 minutes. The product is extracted with chloroform. The latter is washed with water, dried, filtered and evaporated. The residue is distilled, yielding α-hydroxy-p-tolyl 2-thienyl ketone; b.p. 180°-190° C at 0.2 mm. pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04064132
출처 데이터셋uspto-grants-1977_12
ORD IDord-5d42458fb58245b4934df8044450c883
출처 메모uspto-grants-1977_12