Hydrochloric Acid → HCID 23463330, compound
Reaction equation
[F:1][C:2]([F:16])([F:15])[CH2:3][N:4]1[C:8](=[O:9])[CH2:7][C:6]([C:10]([O:12]CC)=[O:11])=[N:5]1.Cl>[OH-].[Na+]>[F:16][C:2]([F:1])([F:15])[CH2:3][N:4]1[C:8](=[O:9])[CH2:7][C:6]([C:10]([OH:12])=[O:11])=[N:5]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.38 Mole (100 g) of 1-(2',2',2'-trifluoroethyl)-3-carbethoxy-2-pyrazolin-5-one were stirred for 1 hour at 90°-95° C. in 900 ml of 1 N sodium hydroxide. The mixture was acidified to pH 1 with concentrated hydrochloric acid and left standing overnight. The precipitate formed was filtered off and rinsed with water
Workup
- waitleft
- customThe precipitate formed
- filtrationwas filtered off
- washrinsed with water
Sources & evidence
- ORD record
- ord-30109c300e7d48bc880201618cadd490
- Source dataset
- uspto-grants-1981_05
- Patent number
- US04266014
Reaction notes
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