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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539309생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/539309

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Potassium tert-butoxideHCID 23665647—
반응물6'-Bromo-4-hydroxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 58197033—
반응물5'-Methylspiro[chromane-4,2'-imidazole]-4',6-diamineHCID 67979407—
용매WaterHCID 962—
용매2-MethyltetrahydrofuranHCID 7301—
용매Sodium chloride; waterHCID 57417360—
생성물6'-bromo-4-ethoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 5819699236%

반응 단계

6′-Bromo-4-hydroxyspiro[cyclohexane-1,2′-inden]-1′(3′H)-one as a 2:1 mixture of isomers (Intermediate 5 Step 2, 10.4 g, 34.1 mmol) and ethyl iodide (3.6 mL, 44.3 mmol) were dissolved in 2-MeTHF (100 mL) under N2. KOt-Bu (7.65 g, 68.2 mmol) was added portionwise to the reaction mixture, keeping the internal temperature below 30° C. The solution was stirred at r.t. overnight. Water (40 mL) and brine (25 mL) were added and the mixture was further stirred for min. The mixture was diluted with brine and 2-Me-THF until two layers formed. The phases were separated. Activated charcoal was added to the organic layer which was then stirred for 10 min. Diatomaceous earth was added and the mixture was further stirred for 5 min. The mixture was filtered through a plug of silica gel and diatomaceous earth, which was rinsed with heptane/EtOAc 7:3. The filtrate was concentrated. The filtration sequence was repeated, affording 4.0 g (36% yield) of the title compound (as a 2:1 mixture of isomers): 1H NMR (300 MHz, CDCl3) δ ppm 1.22 (t, 3 H), 1.32-1.45 (m, 2 H), 1.45-1.52 (m, 2 H), 1.77 (dt, 2 H), 2.07-2.16 (m, 2 H), 2.98 (s, 2 H), 3.30-3.40 (m, 1 H), 3.57 (q, 2 H), 7.34 (d, 1 H), 7.69 (dd, 1 H), 7.87 (d, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865911B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-3195038cec8e4af985784ae452e752db
출처 메모uspto-grants-2014_10