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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705317Generated: October 26, 2026

Bisphenol A → HCID 71257395, compound

https://huagongshe.com/reaction/705317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBisphenol AHCID 6623—
ReactantSodium hydrideHCID 24758—
Reactant(R)-(+)-4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolaneHCID 2734443—
SolventDimethylformamideHCID 6228—
ProductHCID 71257395HCID 7125739523.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173939B2
Source datasetuspto-grants-2015_11
ORD IDord-5bb38725d5aa4f0d868f2a52c4e30619
Source noteuspto-grants-2015_11