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HRID 397162作成日:2026年10月24日

1,4-Dioxaspiro[4.5]decan-8-one → 8-[(4-Fluorophenyl)methylene]-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/ja/reaction/397162

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
反応物(4-Fluorobenzyl)triphenylphosphonium chlorideHCID 2733554—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物8-[(4-Fluorophenyl)methylene]-1,4-dioxaspiro[4.5]decaneHCID 1213395079.3%

反応条件

温度0 °C

反応手順

To a stirring solution of 4-fluorophenylmethyl triphenylphosphonium chloride (39 g, 96 mmol, Lancaster) in 500 mL of dry THF at −78° C. was added 1 M potassium t-butoxide in THF (106 mL, 106 mmol, Aldrich). The reaction was stirred for 30 min and then warmed to 0° C. The reaction was stirred for 30 min and then 1,4-cyclohexanedione mono-ethylene ketal (15.0 g, 96 mmol, Aldrich) was added. After 30 min, the reaction was warmed to room temperature and allowed to stir overnight. The reaction was heated to reflux for 4 h and then cooled to room temperature. The reaction was quenched with saturated ammonium chloride (500 mL) and ethyl acetate (500 mL). The organic layer was separated, washed with brine, dried over sodium sulfate, and conc in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, 19:1 hexanes:ethyl acetate) to yield 18.9 g of a colorless oil. MS (ESI) 251 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06608227B1
出典データセットuspto-grants-2003_08
ORD IDord-157c8a3c8a5045bd96f3c3605b092e44
出典メモuspto-grants-2003_08