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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964187Generated: October 31, 2026

2-Chlorophenol → HCID 131720718, compound

https://huagongshe.com/reaction/964187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorophenolHCID 7245—
ReactantMethylhydroquinoneHCID 7253—
ReactantHCID 18405874HCID 18405874—
CatalystBisphenol AHCID 6623—
CatalystTetrabutylammonium tetraphenylborateHCID 3084234—
ProductHCID 131720718HCID 131720718107.7%

Reaction Steps

Methylhydroquinone (1.95 moles, 242.1 g), bisphenol-A (0.05 moles, 11.41 g), chlorophenyl carbonate (2.06 moles, 582.8 g) and tetrabutylammonium tetraphenylborate (1.6 mmol, 0.899 g) were added to a 1L 3-neck flask and melted at 165° C. with overhead stirring. 89 wt % chlorophenol (3.52 mole, 365 mL) was collected by distillation at about 220° C. followed by a slight vacuum at 230° C. The molten prepolymer was quickly poured onto a foil-lined pyrex dish to obtain a solid (370 g). Subsequent polymerization took place in a 2CV Helicone reactor (500 mL capacity). The prepolymer (200 g) was added at 300° C. and stirred slowly until molten. Once molten, vacuum was applied and the system heated to 330° C. (stirrer setting=7.5). After about 10 minutes, the vacuum reached about 2.0 mm Hg. The polymer was extruded after about 20 minutes to obtain about 120 g of brittle light pink strands (flexible in clear areas and brittle in cloudy areas).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767225
Source datasetuspto-grants-1998_06
ORD IDord-e63eb0cccad94c528a8d694ad34bbcba
Source noteuspto-grants-1998_06