2-Chlorophenol → HCID 131720718, compound

HRID 964186Notes

Reaction equation

HRID 964186 reaction equation
C[C:2]1[CH:8]=[C:7]([OH:9])[CH:6]=[CH:5][C:3]=1[OH:4].[C:10](=O)([O-])[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1Cl.Cl[C:22]1[CH:27]=CC=C[C:23]=1O>C1([B-](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C([N+](CCCC)(CCCC)CCCC)CCC.OC1C=CC(C(C2C=CC(O)=CC=2)(C)C)=CC=1>[CH3:23][C:22]([C:7]1[CH:6]=[CH:5][C:3]([OH:4])=[CH:2][CH:8]=1)([C:15]1[CH:14]=[CH:13][C:12]([OH:11])=[CH:17][CH:16]=1)[CH3:27].[CH3:10][O:9][C:7]1[CH:8]=[CH:2][C:3]([OH:4])=[CH:5][CH:6]=1

Participants

6

Reactant 3

HCID 72452-ChlorophenolHCID 7253MethylhydroquinoneHCID 18405874HCID 18405874, compound

Product 1

HCID 131720718HCID 131720718, compoundYield 110.2%

Reagents, catalysts & solvents 2

HCID 6623Bisphenol ACatalystHCID 3084234Tetrabutylammonium tetraphenylborateCatalyst

Procedure

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).

Workup

  1. customfollowed by a slight vacuum at 230° C
  2. additionThe molten prepolymer was quickly poured onto a foil-lined pyrex dish

Sources & evidence

ORD record
ord-604b0b40081b463d90085317ad853f3d
Source dataset
uspto-grants-1998_06
Patent number
US05767225

Reaction notes

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