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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 705317생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Bisphenol AHCID 6623—
반응물Sodium hydrideHCID 24758—
반응물(R)-(+)-4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolaneHCID 2734443—
용매DimethylformamideHCID 6228—
생성물(S)-4-(2-(4-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)phenyl)propan-2-yl)phenolHCID 7125739523.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09173939B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-5bb38725d5aa4f0d868f2a52c4e30619
출처 메모uspto-grants-2015_11