戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 539267作成日:2026年10月27日

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

https://huagongshe.com/reaction/539267

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl iodideHCID 6328—
反応物Potassium tert-butoxideHCID 23665647—
反応物6'-Bromo-4-hydroxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 58197033—
溶媒TetrahydrofuranHCID 8028—
生成物6'-bromo-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-oneHCID 5819726394%

反応条件

温度0 °C

反応手順

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:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865911B2
出典データセットuspto-grants-2014_10
ORD IDord-f1b4bb01eb1e42c190d2186f5b90d2af
出典メモuspto-grants-2014_10