Methacrylic Acid → 2-Methyl-4-oxatricyclo[5.2.1.02,6]decan-3-yl methacrylate

HRID 601739

Reaktionsgleichung

Reaktionsgleichung von HRID 601739
C(O[CH:5]1[O:13][CH2:12][CH:11]2[C:6]1([CH3:15])[CH:7]1[CH2:14][CH:10]2[CH2:9][CH2:8]1)(=O)C.[C:16]([OH:21])(=[O:20])[C:17]([CH3:19])=[CH2:18]>C(C1C(O)=C(C(C)(C)C)C=C(C)C=1)C1C(O)=C(C(C)(C)C)C=C(C)C=1>[C:16]([O:21][CH:5]1[O:13][CH2:12][CH:11]2[C:6]1([CH3:15])[CH:7]1[CH2:14][CH:10]2[CH2:9][CH2:8]1)(=[O:20])[C:17]([CH3:19])=[CH2:18]

Komponenten

4

Edukt 2

HCID 4093Methacrylic AcidHCID 669308112-Methyl-4-oxatricyclo[5.2.1.02,6]decan-3-yl acetate

Produkt 1

HCID 669307992-Methyl-4-oxatricyclo[5.2.1.02,6]decan-3-yl methacrylateAusbeute 91 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 83982,2'-Methylenebis(4-methyl-6-tert-butylphenol)Katalysator

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A mixture of 73 g of 2-methyl-4-oxatricyclo[5.2.1.02,6]-decan-3-yl acetate, 150 g of methacrylic acid, and 40 mg of 2,2′-methylenebis(6-t-butyl-p-cresol) was heated at 50° C. under atmospheric pressure for 30 minutes, after which under a reduced pressure of 0.20 kPa, the reaction mixture was heated for 18 hours for distilling off the acetic acid formed. The reaction mixture was purified by distillation, obtaining 72 g (yield 91%) of the target compound.

Aufarbeitung

  1. temperatureafter which under a reduced pressure of 0.20 kPa, the reaction mixture was heated for 18 hours
  2. distillationfor distilling off the acetic acid
  3. customformed
  4. distillationThe reaction mixture was purified by distillation

Quellen und Nachweise

ORD-Eintrag
ord-a4e26a2840e440c09d215439599b115c
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07902385B2

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