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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 888295생성일: 2026년 10월 26일

Water → 8-(4-(4-Methoxyphenyl)-5-(p-tolyl)thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/888295

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
반응물8-(4-(4-Methoxyphenyl)-5-(p-tolyl)thiazol-2-yl)-1,4-dioxaspiro[4.5]decaneHCID 67296392—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매ButyllithiumHCID 178418339—
생성물8-(4-(4-Methoxyphenyl)-5-(p-tolyl)thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-olHCID 6729642455%

반응 단계

To a solution of 8-(4-(4-methoxyphenyl)-5-(p-tolyl)thiazol-2-yl)-1,4-dioxaspiro[4.5]decane (Reference Example 95) (734 mg, 1.74 mmol) in tetrahydrofuran (8.7 mL), 1.63 M n-butyllithium/solution in n-hexane (1.17 mL) was added at −78° C., and the obtained solution was stirred at the same temperature for 1 hour. The reaction solution was added at −78° C. to a solution of 3-phenyl-2-(phenylsulfonyl)-1,2-oxaziridine (546 mg, 2.09 mmol) in tetrahydrofuran (8.7 mL), and the obtained solution was allowed to warm gradually to room temperature with stirring. Distilled water was added to the reaction solution, and the resulting solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate) to obtain the captioned compound (417 mg, 0.954 mmol, 55%) as a colorless amorphous product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247569B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-5d01bba6dc0f4998b5d7ce065be207e8
출처 메모uspto-grants-2012_08