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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132674생성일: 2026년 10월 26일

Ammonium Chloride → 8-[4-(4,4-Dimethyl-4,5-dihydro-1,3-oxazol-2-yl)phenyl]-1,4-dioxaspiro[4,5]decan-8-ol

https://huagongshe.com/reaction/132674

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-(4-Bromophenyl)-4,4-dimethyl-4,5-dihydrooxazoleHCID 403395—
반응물1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
용매TetrahydrofuranHCID 8028—
생성물8-[4-(4,4-Dimethyl-4,5-dihydro-1,3-oxazol-2-yl)phenyl]-1,4-dioxaspiro[4,5]decan-8-olHCID 59836702—

반응 단계

A solution of 8 g of 2-(4-bromophenyl)-4,4-dimethyl-4,5-dihydro-1,3-oxazole (31.5 mmol) in 15 ml of anhydrous THF is poured dropwise onto 956 mg of Mg (39.3 mmol) in such a way as to maintain the mixture at the reflux temperature and the mixture is refluxed for 2.5 hours. The mixture is cooled to room temperature and a solution of 5.41 g of 1,4-cyclohexandione monoethyleneacetal (34.65 mmol) in 20 ml of anhydrous THF is added to it dropwise. The mixture is stirred at room temperature for 1.5 hours and then at reflux temperature for 1 hour. The mixture is poured into 500 ml of a 10% NH4Cl solution and extracted with ethyl acetate. The organic phase is dried and, after filtration, the solvent is evaporated off under reduced pressure. The residue is crystallized in ethyl acetate. The product of the title is obtained in the form of a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388031B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-e74c7a91e3f24a36955ec31da46d9a1c
출처 메모uspto-grants-2008_06