Reaction equation
I[CH2:2][CH2:3][CH2:4][CH3:5].[OH:6][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[CH:13]=[C:12]([CH:17]([CH3:21])[C:18]([OH:20])=[O:19])[CH:11]=[CH:10]2>>[CH3:21][CH:17]([C:12]1[CH:11]=[CH:10][C:9]2[C:14](=[CH:15][CH:16]=[C:7]([O:6][CH2:2][CH2:3][CH2:4][CH3:5])[CH:8]=2)[CH:13]=1)[C:18]([OH:20])=[O:19]Participants
3
Procedure
The title compound is prepared according to the method of Example 7 using 1-iodobutane and racemic 6-hydroxy-α-methyl-2-naphthaleneacetic acid. White crystals are obtained having a melting point of 125°-127° c.
Workup
- customWhite crystals are obtained
Sources & evidence
- ORD record
- ord-c1989b72b73c4f8785cdadddbaec055c
- Source dataset
- uspto-grants-1993_05
- Patent number
- US05208344
Linked notes
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