Sodium Hydroxide → HCID 67914037, compound
Reaction equation
[ClH:1].[CH:2]1[C:12]2[C:11](=[C:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][CH2:21][CH2:22][C:23]([O:25]CC)=[O:24])[CH2:15][CH2:14]3)[C:10]3[CH:28]=[CH:29][CH:30]=[CH:31][C:9]=3[CH2:8][O:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>CO>[ClH:1].[CH:2]1[C:12]2[C:11](=[C:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][CH2:21][CH2:22][C:23]([OH:25])=[O:24])[CH2:15][CH2:14]3)[C:10]3[CH:28]=[CH:29][CH:30]=[CH:31][C:9]=3[CH2:8][O:7][C:6]=2[CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4.20 g of ethyl 4-(dibenz[b,e]oxepin-11(6H)-ylidene)-1-piperidinevalerate hydrochloride, 14.5 ml of 2N sodium hydroxide aqueous solution and 40 ml of methanol was refluxed for 1 hr and concentrated. Water was added to the residue, adjusted to pH 2 with 10% hydrochloric acid. The precipitate was collected by filtration and washed with water and ether to give 3.92 g of colorless crystals, which were recrystallized from water to give 3.08 g of colorless prisms, mp 304°-306° C. (dec.).
Workup
- temperaturewas refluxed for 1 hr
- concentrationconcentrated
- additionWater was added to the residue
- filtrationThe precipitate was collected by filtration
- washwashed with water and ether
Sources & evidence
- ORD record
- ord-3790930e6f5342a58bf5dbaff273c29e
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05095022
Reaction notes
Loading…