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HRID 1965074作成日:2026年10月26日

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

https://huagongshe.com/reaction/1965074

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Potassium tert-butoxideHCID 23665647—
反応物6'-Bromo-4-hydroxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 58197033—
反応物5'-Methylspiro[chromane-4,2'-imidazole]-4',6-diamineHCID 67979407—
溶媒WaterHCID 962—
溶媒2-MethyltetrahydrofuranHCID 7301—
溶媒Sodium chloride; waterHCID 57417360—
生成物6'-bromo-4-ethoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 5819699236%

反応手順

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 5 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) 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415483B2
出典データセットuspto-grants-2013_04
ORD IDord-e4fbf70d648043c3bc7f215bf2888c81
出典メモuspto-grants-2013_04