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HRID 705317作成日:2026年10月26日

Bisphenol A → (S)-4-(2-(4-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)phenyl)propan-2-yl)phenol

https://huagongshe.com/reaction/705317

反応式

関与物質

役割名称HCID仕込み量
反応物Bisphenol AHCID 6623—
反応物Sodium hydrideHCID 24758—
反応物(R)-(+)-4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolaneHCID 2734443—
溶媒DimethylformamideHCID 6228—
生成物(S)-4-(2-(4-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)phenyl)propan-2-yl)phenolHCID 7125739523.7%

反応手順

Sodium hydride (60% dispersion in mineral oil, 1750 mg, 43.80 mmol, 1.0 equiv) was added slowly to a stirred solution of Bisphenol A (10000 mg, 43.80 mmol, 1 equiv) in anhydrous dimethyl formamide (30 mL), at room temperature, and the contents were stirred under an atmosphere of argon for 20 min. (R)-(+)-4-chloromethyl-2,2-dimethyl-1,3-dioxolane 98% (7.10 mL, 52.56 mmol, 1.2 equiv) was added via syringe and the mixture was allowed to react at 70-80° C. for 40 h. Then, the reaction was quenched by the addition of a saturated solution of ammonium chloride (10 mL), and the mixture was extracted with ethyl acetate (3×20 mL). The organic layer was washed with deionized water (25 mL), dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by flash column chromatography on silica gel (eluent: 10% ethyl acetate in hexane) to provide the title compound (3560 mg, 24%, 25-30% conversion) as a foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09173939B2
出典データセットuspto-grants-2015_11
ORD IDord-5bb38725d5aa4f0d868f2a52c4e30619
出典メモuspto-grants-2015_11