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Potassium Hydroxide → 3-(4'-Fluoro-4-biphenylyl)-3-methyl-pyrazolidin-5-one

HRID 1576424
Notes
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Reaction equation

HRID 1576424 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14]3([CH3:20])[CH2:18][C:17](=N)[NH:16][NH:15]3)=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[OH-:21].[K+]>C(O)(C)C>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14]3([CH3:20])[CH2:18][C:17](=[O:21])[NH:16][NH:15]3)=[CH:10][CH:9]=2)=[CH:4][CH:3]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14797Potassium HydroxideHCID 1784215893-(4'-Fluoro-4-biphenylyl)-3-methyl-5-imino-pyrazolidine

Product 1

HCID 215126753-(4'-Fluoro-4-biphenylyl)-3-methyl-pyrazolidin-5-one

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Procedure

26.9 g of 3-(4'-fluoro-4-biphenylyl)-3-methyl-5-imino-pyrazolidine are boiled for 10 minutes with 150 ml of 2 N aqueous potassium hydroxide solution and 150 ml of isopropanol and the mixture is worked up in the usual manner to give 3-(4'-fluoro-4-biphenylyl)-3-methyl-pyrazolidin-5-one, m.p. 194°-196°.

On this pageParticipantsProcedureSources & evidenceReaction notes

Sources & evidence

ORD record
ord-dd4f61f3730042448d52a7f3cc046c07
Source dataset
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03980795

Reaction notes

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