Reaction equation
C1CCC(N=C=NC2CCCCC2)CC1.[C:16](=[C:19]1[CH2:22][CH:21]([C:23]([O-:25])=[O:24])[CH2:20]1)([CH3:18])[CH3:17].[CH2:26]([C@H:29]1[CH2:34][CH2:33][C@H:32]([C:35]2[CH:40]=[CH:39][C:38](O)=[CH:37][CH:36]=2)[CH2:31][CH2:30]1)[CH2:27][CH3:28]>ClCCl>[C:16](=[C:19]1[CH2:22][CH:21]([C:23]([O:25][C:38]2[CH:37]=[CH:36][C:35]([C@H:32]3[CH2:33][CH2:34][C@H:29]([CH2:26][CH2:27][CH3:28])[CH2:30][CH2:31]3)=[CH:40][CH:39]=2)=[O:24])[CH2:20]1)([CH3:18])[CH3:17]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 0.11 mol of DCC add 50 ml of dichloromethane is added at 0° C. to a mixture of 0.1 mol of 3-isopropylidenecyclobutanecarboxylate [sic] (prepared by the method of Gripps et al., Am. Soc. 81 (1959), 2723-2728) 0.1 mol of 4-(trans-4-propylcyclohexyl)phenol and 100 ml of dichloromethane. After the mixture has been stirred at room temperature for 16 hours and the solid constituents have been removed, conventional work-up gives the product.
Workup
- customprepared by the method of Gripps et al., Am
- customthe solid constituents have been removed
- customconventional work-up gives the product
Sources & evidence
- ORD record
- ord-f3dec78be4c34ba098fbc50fb0163095
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05384072
Linked notes
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