Calcium Hydroxide → HCID 23316677, compound
Reaction equation
[O:1]=[C:2]1[N:9]2[CH:5]([CH2:6][CH2:7][C:8]2=[O:10])[CH2:4][CH:3]1[C:11]([OH:13])=[O:12].[OH-].[Ca+2:15].[OH-]>O1CCOCC1>[Ca+2:15].[O:1]=[C:2]1[N:9]2[CH:5]([CH2:6][CH2:7][C:8]2=[O:10])[CH2:4][CH:3]1[C:11]([O-:13])=[O:12].[O:1]=[C:2]1[N:9]2[CH:5]([CH2:6][CH2:7][C:8]2=[O:10])[CH2:4][CH:3]1[C:11]([O-:13])=[O:12].[O:1]=[C:2]1[N:9]2[CH:5]([CH2:6][CH2:7][C:8]2=[O:10])[CH2:4][CH:3]1[C:11]([OH:13])=[O:12]Participants
5
Procedure
A solution of hexahydro-3,5-dioxo-1H-pyrrolizine-2-carboxylic acid (8.3 g, 0.1 mole) in dioxane (200 ml) at 0° C. is treated with 0.1N calcium hydroxide solution (100 ml, 0.1 mole) and the resulting solution of the calcium salt of hexahydro-3,5-dioxo-1H-pyrrolizine-2-carboxylic acid is concentrated at reduced pressure to yield the dry calcium salt of hexahydro-3,5-dioxo-1H-pyrrolizine-2-carboxylic acid.
Workup
- concentrationthe resulting solution of the calcium salt of hexahydro-3,5-dioxo-1H-pyrrolizine-2-carboxylic acid is concentrated at reduced pressure
Sources & evidence
- ORD record
- ord-b6a15b87b7e14fe7881ffc4f149372bf
- Source dataset
- uspto-grants-1985_11
- Patent number
- US04551470
Reaction notes
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