Phenol → HCID 20525897, compound
Reaction equation
[CH2:1]([NH:17][C:18]1[CH:28]=[CH:27][C:21]([CH2:22][CH2:23][C:24]([OH:26])=[O:25])=[CH:20][CH:19]=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][CH2:14][CH2:15][CH3:16].C(N1C=CN=C1)(N1C=CN=C1)=O.[C:41]1(O)[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1.[H-].[Na+]>O1CCCC1>[CH2:1]([NH:17][C:18]1[CH:19]=[CH:20][C:21]([CH2:22][CH2:23][C:24]([O:26][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)=[O:25])=[CH:27][CH:28]=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][CH2:14][CH2:15][CH3:16]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 0.05 mole of 4-(hexadecylamino)hydrocinnamic acid and 0.05 mole of 1,1'-carbonyldiimidazole in 50 ml. of tetrahydrofuran is treated with 0.052 mole of phenol and a trace of sodium hydride. The reaction is heated to reflux for 3 hours, then cooled, filtered and evaporated in vacuo providing phenyl 4-(hexadecylamino)hydrocinnamate.
Workup
- temperatureThe reaction is heated
- temperatureto reflux for 3 hours
- temperaturecooled
- filtrationfiltered
- customevaporated in vacuo
Sources & evidence
- ORD record
- ord-860c6ac6c7244512950ac7540aa55d53
- Source dataset
- uspto-grants-1982_09
- Patent number
- US04348399
Reaction notes
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