Water → Acetic Acid 12-(4-Formyl-phenoxy)-dodecyl Ester
Reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][O:14][C:15]1[CH:22]=[CH:21][C:18]([CH:19]=[O:20])=[CH:17][CH:16]=1.O.[C:24](OC(=O)C)(=[O:26])[CH3:25]>>[CH:19]([C:18]1[CH:17]=[CH:16][C:15]([O:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][O:1][C:24](=[O:26])[CH3:25])=[CH:22][CH:21]=1)=[O:20]Participants
4
Procedure
4-(12-Hydroxyl-dodecyloxy)-benzaldehyde (1.1 g, 3.6 mmol, see Example 2 above) was heated at reflux in acetic anhydride (15 ml) for 90 minutes. After cooling, the solution was poured into water with stirring. The title compound formed as a precipitate which was collected by filtration, washed with water and dried.
Workup
- temperatureAfter cooling
Sources & evidence
- ORD record
- ord-f8fc0837b3a749fabb70322c2da38585
- Source dataset
- uspto-grants-2003_10
- Patent number
- US06630128B1
Reaction notes
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