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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981370Generated: October 30, 2026

Water → HCID 20072040, compound

https://huagongshe.com/reaction/981370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBisphenol AHCID 6623—
ReactantPerfluorocyclopenteneHCID 11212—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 20072040HCID 20072040—

Reaction Steps

45.6 of bisphenol A (0.2 mol) were dissolved in 100 ml of methanol with warming and 36 g of a 30% strength by weight sodium methoxide solution were added. The mixture was evaporated to dryness on a rotary evaporator, 61 g of monosodium bisphenol A remaining. This was dissolved in 100 ml of dimethylformamide, 21.2 g of perfluorocyclopentene (0.1 mol) were added at 5° C. in the course of 60 minutes, then the mixture was warmed to room temperature and stirred at room temperature for 18 hours. It was then warmed to 70° C. for 2 hours. The mixture was then stirred into 200 ml of water and the organic phase was separated off. The latter was taken up in methylene chloride, and the solution was washed with 100 ml of water, then with 50 ml of 5% strength by weight hydrochloric acid and then again with 100 ml of water and then dried. After stripping off the solvent on a rotary evaporator and drying in the vacuum of an oil pump at 100° C., 53 g of a glass-like, transparent residue remained, which corresponds to 90.7% of theory. The 19F nuclear magnetic resonance spectrum showed characteristic bands at δ=-36.1 ppm and at δ=-51.5 ppm, measured against trifluoroacetic acid as external standard.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990633
Source datasetuspto-grants-1991_02
ORD IDord-2386525c91b74b2fac44a2272f9e48b2
Source noteuspto-grants-1991_02