Hydrochloric Acid → HCID 21955396, compound
Reaction equation
[C:1]([O:5][C:6](=[O:31])[CH2:7][CH:8]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[C:12](=[O:19])[N:11]([CH2:20][CH2:21][C:22]([O:24]CC)=[O:23])[C:10]2[CH:27]=[CH:28][CH:29]=[CH:30][C:9]1=2)([CH3:4])([CH3:3])[CH3:2].[Li+].[OH-].Cl.C(Cl)Cl>O1CCOCC1.O>[C:1]([O:5][C:6](=[O:31])[CH2:7][CH:8]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[C:12](=[O:19])[N:11]([CH2:20][CH2:21][C:22]([OH:24])=[O:23])[C:10]2[CH:27]=[CH:28][CH:29]=[CH:30][C:9]1=2)([CH3:4])([CH3:2])[CH3:3]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 3-[11-(2-tert-butoxy-2-oxoethyl)-6-oxo-6,11-dihydro-5-H-dibenzo[b,e]azepin-5-yl]propanoate 5 (2.55 g, 6.02 mmol) was dissolved in 15 ml of 2:1 dioxane/H2O and, after addition of 0.17 g of LiOH, stirred at RT. After the reaction was complete, the mixture was acidified with 2N HCl and, after addition of CH2Cl2, washed with saturated NaCl solution, dried and concentrated.
Workup
- washwashed with saturated NaCl solution
- customdried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-093c313c00444b609ad689a0d93eb484
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07105508B1
Reaction notes
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