HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964186Generated: October 31, 2026
2-Chlorophenol → HCID 131720718, compound
https://huagongshe.com/reaction/964186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorophenol | HCID 7245 | — |
| Reactant | Methylhydroquinone | HCID 7253 | — |
| Reactant | HCID 18405874 | HCID 18405874 | — |
| Catalyst | Bisphenol A | HCID 6623 | — |
| Catalyst | Tetrabutylammonium tetraphenylborate | HCID 3084234 | — |
| Product | HCID 131720718 | HCID 131720718 | 110.2% |
Reaction Steps
Methylhydroquinone (1.9 moles, 235.87 g), bisphenol-A (0.1 moles, 22.83 g), chlorophenyl carbonate (2.04 moles, 577.12 g) and tetrabutylammonium tetraphenylborate (1.6 mmol, 0.899 g) were added to a 1 L 3-neck flask and melted at 165° C. with overhead stirring. 85 wt % chlorophenol (3.38 mole, 350 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 (369 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 about 325° C. (stirrer setting=6.5). After about 10 minutes, the vacuum reached about 2.5 mm Hg. The polymer was extruded after 25 minutes to obtain about 122 g of light pink strands (flexible in clear areas and brittle in cloudy areas).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05767225 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-604b0b40081b463d90085317ad853f3d |
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| Source note | uspto-grants-1998_06 |
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