Reaktionsgleichung
C(Cl)(=O)C.[C:5]1([CH2:15][C:16]([OH:18])=[O:17])([CH2:11][C:12]([OH:14])=O)[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1>>[C:5]12([CH2:11][C:12](=[O:14])[O:18][C:16](=[O:17])[CH2:15]1)[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10]2Komponenten
3
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
Acetyl chloride (35 m, 492 mmol) was added to 1,1-cyclohexanediacetic acid (25 g, 125 mmol) in a round bottom flask and the suspension was heated for 3 hrs. at 60° C. using an oil bath. After about 15 min. the suspension became clear. The reaction was attached to a short path condenser and was heated to 100° C. under vacuum to remove volatile by products. 1HNMR indicated no starting diacid and GC indicated >99% purity. Upon cooling to room temperature the anhydride solidified. 1H NMR (CDCl3): 62.65(s,4H); 1.45(m,10H)
Aufarbeitung
- temperaturethe suspension was heated for 3 hrs
- customat 60° C.
- customThe reaction was attached to a short path condenser
- customto remove volatile by products
- temperatureUpon cooling to room temperature the anhydride
Quellen und Nachweise
- ORD-Eintrag
- ord-586f30653bcf4a66af018a6efb9bb7ea
- Quelldatensatz
- uspto-grants-1990_03
- Patentnummer
- US04908475
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