戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 275398作成日:2026年10月27日

3,6-Dioxabicyclo[3.1.0]hexane → trans-4-[[3,5-bis (1,1-Dimethylethyl)-4-hydroxyphenyl]thio]tetrahydro-3-furanol

https://huagongshe.com/reaction/275398

反応式

関与物質

役割名称HCID仕込み量
反応物3,6-Dioxabicyclo[3.1.0]hexaneHCID 67511—
反応物2,6-Di-tert-butyl-4-mercaptophenolHCID 70370—
生成物trans-4-[[3,5-bis (1,1-Dimethylethyl)-4-hydroxyphenyl]thio]tetrahydro-3-furanolHCID 15224688—

反応手順

2,6-bis(1,1-Dimethylethyl)-4-mercaptophenol (1.85 g, 0.0078 mole) and the compound of Example 1 (0.64 g, 0.0074 mole) were added to a degassed (Argon) solution of 50% sodium hydroxide (5 ml) and isopropyl alcohol (50 ml). The reaction was heated to reflux for 24 hours. The reaction was cooled to room temperature and poured into water (125 ml). The solution was made acidic with 1N hydrochloric acid and extracted 3 times with 100 ml of diethyl ether. The combined diethyl ether extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to an oily solid in a rotary evaporator. The product was purified by silica gel chromatography and recrystallized from hexane (m.p. ca. 104° C.). The structure was supported by NMR and infrared spectroscopy and elemental analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05393764
出典データセットuspto-grants-1995_02
ORD IDord-ae51ef06620140888809b2972abd90c6
出典メモuspto-grants-1995_02