4-Hydroxybenzoic Acid → HCID 54110816, compound
Reaction equation
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[CH3:11][C@@H:12]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[C:13](Cl)=[O:14]>>[CH3:11][C@@H:12]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[C:13]([O:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1)=[O:14]Participants
3
Procedure
Using p-hydroxybenzoic acid (3.25 g, 23.5 mmol) and (S)-2-methyldecanoylchloride (4.83 g, 23.6 mmol), the reaction was carried out in the same manner as described in Example 4, (1}, to give 2.35 g of the title compound as white crystals; mp. 92.5°-96.5° C.
Sources & evidence
- ORD record
- ord-126b150e7e8e498e91f8fa27f92e85bb
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05128062
Reaction notes
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