4-Nitrophenol → HCID 54238477, compound
Reaction equation
[CH2:1]([C:6]([CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])=[CH:7][CH:8]=[CH:9][C:10]([OH:12])=[O:11])[CH2:2][CH2:3][CH2:4][CH3:5].[N+:18]([C:21]1[CH:26]=[CH:25][C:24](O)=[CH:23][CH:22]=1)([O-:20])=[O:19].C1(N=C=NC2CCCCC2)CCCCC1>ClCCl>[N+:18]([C:21]1[CH:26]=[CH:25][C:24]([O:11][C:10](=[O:12])[CH:9]=[CH:8][CH:7]=[C:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])[CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])=[CH:23][CH:22]=1)([O-:20])=[O:19]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
As in Example 115, 5-pentyl-2,4-decadienoic acid (4.0 g) and 4-nitrophenol (2.8 g) in 30 mL of dichloromethane was treated with 1,3-dicyclohexylcarbodiimide (3.48 g) and the mixture was stirred at room temperature for 18 hours. After the usual work up, the crude ester was Purified by HPLC (ether-hexane; 1:24) to furnish 2,45 g of 5-pentyl-2,4-decadienoic acid 4-nitrophenyl ester as an oil.
Workup
- customAfter the usual work up, the crude ester was Purified by HPLC (ether-hexane; 1:24)
Sources & evidence
- ORD record
- ord-83c2c09a51e646ff813c1e03b7b7a50c
- Source dataset
- uspto-grants-1990_12
- Patent number
- US04975438
Reaction notes
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