Sodium Hydroxide → HCID 60003039, compound
Reaction equation
[C:1]([C:5]1[C:14]2[CH:13]=[C:12](/[C:15](/[CH2:28][CH3:29])=[C:16](/[F:27])\[CH:17]=[CH:18]\[C:19](\[CH3:26])=[CH:20]\[C:21]([O:23]CC)=[O:22])[C:11]([O:30][CH2:31][CH3:32])=[CH:10][C:9]=2[C:8]([CH3:34])([CH3:33])[CH2:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>C1COCC1.C(O)C>[C:1]([C:5]1[C:14]2[CH:13]=[C:12](/[C:15](/[CH2:28][CH3:29])=[C:16](/[F:27])\[CH:17]=[CH:18]\[C:19](\[CH3:26])=[CH:20]\[C:21]([OH:23])=[O:22])[C:11]([O:30][CH2:31][CH3:32])=[CH:10][C:9]=2[C:8]([CH3:33])([CH3:34])[CH2:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
As described in General Procedure J-1, ethyl (2E,4E,6E)-7-(8-tert-butyl-3-ethoxy-5,5-dimethyl-5,6-dihydronaphthalen-2-yl)-6-fluoro-3-methyl-nona-2,4,6-trienoate (Compound A-74, 520 mg, 1.111 mmol) in THF (5 mL) and ethanol (5 mL) was hydrolyzed with 1.5 N NaOH (5 mL) to produce the title compound as a yellow solid after purification by recrystallization from acetonitrile.
Sources & evidence
- ORD record
- ord-0ab746b1a8a54544821ea4fdffcb386e
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06887896B1
Reaction notes
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