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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539267생성일: 2026년 10월 26일

Water → 6'-bromo-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-one

https://huagongshe.com/reaction/539267

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl iodideHCID 6328—
반응물Potassium tert-butoxideHCID 23665647—
반응물6'-Bromo-4-hydroxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 58197033—
용매TetrahydrofuranHCID 8028—
생성물6'-bromo-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 5819726394%

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온도0 °C

반응 단계

A mixture of isomers of 6′-bromo-4-hydroxyspiro[cyclohexane-1,2′-inden]-1′(3′H)-one (Intermediate 5 Step 2, 12.7 g, 43.0 mmol) was dissolved in THF (210 mL) under N2 and cooled to 0° C. Potassium tert-butoxide (5.79 g, 51.6 mmol) was added portionwise and the mixture was stirred at 0° C. for 25 min. Methyl iodide (4.30 mL, 68.8 mmol) was added. The cooling bath was removed, and the mixture was stirred at r.t. Additional potassium tert-butoxide (0.483 g, 4.30 mmol) was added twice, after 2 h and 3 h respectively, and then the mixture was stirred for 2 h. Water (100 mL) was added and the resulting solution was partitioned between aq. NaCl solution (200 mL), and EtOAc (200 mL). The aq. phase was extracted with another portion of EtOAc (100 mL). The combined organic phases were dried (MgSO4) and evaporated to give 12.5 g (94% yield) of a mixture (approx. 80:20) of:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865911B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-f1b4bb01eb1e42c190d2186f5b90d2af
출처 메모uspto-grants-2014_10