Sodium Bicarbonate → HCID 20520801, compound
Reaction equation
[F:1][CH:2]([O:8][C:9]1[CH:21]=[C:20]2[C:12]([C:13]3[C:18]([CH2:22][CH3:23])([CH2:19]2)[CH2:17][CH2:16][C:15](=[O:24])[CH:14]=3)=[C:11]([Cl:25])[C:10]=1[Cl:26])[C:3]([O:5]CC)=[O:4].C(=O)(O)[O-].[Na+]>C(O)C.O>[F:1][CH:2]([O:8][C:9]1[CH:21]=[C:20]2[C:12]([C:13]3[C:18]([CH2:22][CH3:23])([CH2:19]2)[CH2:17][CH2:16][C:15](=[O:24])[CH:14]=3)=[C:11]([Cl:25])[C:10]=1[Cl:26])[C:3]([OH:5])=[O:4]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Ethyl fluoro[(5,6-dichloro-9a-ethyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetate (4.01 gm., 0.02 mole) is dissolved in ethanol (75 ml.) and treated with a solution of sodium bicarbonate (3.36 gm., 0.04 mole) in water (150 ml.). The mixture is heated and stirred on a steam bath for 15 minutes and then concentrated in vacuo to a volume of 50 ml. The residual solution is diluted with water (50 ml.) and acidified to Congo red test paper with 6 normal hydrochloric acid. The precipitate that forms is removed by filtration, washed with water and dried. The product is sufficiently pure for use but it may be further purified by recrystallization from a mixture of acetic acid and water to produce pure fluoro[(5,6-dichloro-9a-ethyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetic acid.
Workup
- temperatureThe mixture is heated
- concentrationconcentrated in vacuo to a volume of 50 ml
- additionThe residual solution is diluted with water (50 ml.)
- customThe precipitate that forms is removed by filtration
- washwashed with water
- customdried
- custommay be further purified by recrystallization from a mixture of acetic acid and water
Sources & evidence
- ORD record
- ord-6c4ceef0483341aa8cef3002cd19eda7
- Source dataset
- uspto-grants-1982_10
- Patent number
- US04356314
Reaction notes
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