Sulfuric Acid → p-Tetrahydropyranylstyrene p-hydroxystyrene

HRID 129368

Reaktionsgleichung

Reaktionsgleichung von HRID 129368
[CH:1]#[C:2][C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1.[O:10]1[CH:15]=[CH:14][CH2:13][CH2:12][CH2:11]1.S(=O)(=O)(O)O>C(COC)OC>[O:10]1[CH2:11][CH2:12][CH2:13][CH2:14][CH:15]1[C:6]1[CH:7]=[CH:8][C:3]([CH:2]=[CH2:1])=[CH:4][CH:5]=1.[OH:9][C:6]1[CH:7]=[CH:8][C:3]([CH:2]=[CH2:1])=[CH:4][CH:5]=1

Komponenten

5

Versuchsvorschrift

To a solution of poly(p-hydroxystyrene) (9.0 g) [MARUKA LYNCUR-M, manufactured by Maruzen Petrochemical Co., Ltd., Mw 10000 and Mn 5000] in dimethoxyethane (100 ml), 3,4-dihydro-2H-pyran (12.6 g) and conc. sulfuric acid (0.5 ml) were added, followed by reaction at 30°-40° C. for 15 hours with stirring. After reaction, the mixture was evaporated in vacuo, the residue was neutralized by addition of sodium carbonate and poured into H2O (1 liter). The precipitate was filtered by suction, washed with H2O and dried under reduced pressure to give 11.0 g of the title compound as a white powder having Mw 10000 (GPC with polystyrene calibration). The composition of the polymer was found to be p-tetrahydropyranyloxystyrene unit and p-hydroxystyrene unit in a molar ratio of ca. 3:7 based on 1HNMR.

Aufarbeitung

  1. customfollowed by reaction at 30°-40° C. for 15 hours
  2. customAfter reaction
  3. customthe mixture was evaporated in vacuo
  4. additionthe residue was neutralized by addition of sodium carbonate
  5. additionpoured into H2O (1 liter)
  6. filtrationThe precipitate was filtered by suction
  7. washwashed with H2O
  8. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-3cb24663ba8949e3889f345c771e8b64
Quelldatensatz
uspto-grants-1995_11
Patentnummer
US05468589

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