Hydrochloric Acid → HCID 14699187, compound
Reaction equation
[OH-].[Na+].C[O:4][C:5](=[O:36])[CH2:6][CH:7]([OH:35])[CH2:8][CH:9]([OH:34])/[CH:10]=[CH:11]/[C:12]1[C:16]2([CH2:20][CH2:19][CH2:18][CH2:17]2)[C:15]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[CH:14][C:13]=1[C:27]1[CH:32]=[CH:31][C:30]([F:33])=[CH:29][CH:28]=1.Cl>C(O)C>[F:33][C:30]1[CH:29]=[CH:28][C:27]([C:13]2[CH:14]=[C:15]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[C:16]3([CH2:20][CH2:19][CH2:18][CH2:17]3)[C:12]=2/[CH:11]=[CH:10]/[CH:9]([OH:34])[CH2:8][CH:7]([OH:35])[CH2:6][C:5]([OH:36])=[O:4])=[CH:32][CH:31]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Aqueous 1N NaOH (13.4 ml, 13.4 mmoles) was added to a 0.2M ethanol solution of the 3,5-dihydroxy ester prepared in Step 7 (4.1 g, 8.9 mmoles). After stirring for 10 minutes, the ethanol was evaporated in vacuo. The residue was redissolved in H2O and the aqueous layer was acidified with 1N HCl (15 ml, 15 mmoles).
Workup
- customthe ethanol was evaporated in vacuo
- dissolutionThe residue was redissolved in H2O
Sources & evidence
- ORD record
- ord-bb6b81bdf4224ab48f553b27c2a9a497
- Source dataset
- uspto-grants-1990_02
- Patent number
- US04904691
Reaction notes
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