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4-(2,3-Dihydroxypropyl)-2-fluorobenzonitrile → 2-Fluoro-4-(2-oxoethyl)benzonitrile

HRID 1519599
Notes
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Reaction equation

HRID 1519599 reaction equation
[OH:1][CH:2](CO)[CH2:3][C:4]1[CH:11]=[CH:10][C:7]([C:8]#[N:9])=[C:6]([F:12])[CH:5]=1>CO.O>[F:12][C:6]1[CH:5]=[C:4]([CH2:3][CH:2]=[O:1])[CH:11]=[CH:10][C:7]=1[C:8]#[N:9]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 675132414-(2,3-Dihydroxypropyl)-2-fluorobenzonitrile

Product 1

HCID 866944782-Fluoro-4-(2-oxoethyl)benzonitrile

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Conditions

Temperature
0 °C

Procedure

A solution of 4-(2,3-dihydroxypropyl)-2-fluorobenzonitrile (500 mg, 2.6 mmol) in 10 mL of methanol and 3 mL of water was cooled to 0° C. by ice bath, then NaIO4 (820 mg, 3.8 mmol) was added and the mixture was stirred at 0° C. for two hours. The reaction was monitored according to TLC. The mixture was filtered and concentrated. The residue was dissolved in DCM, dried over anhydrous sodium sulfate, and then purified by flash column chromatography to give 2-fluoro-4-(2-oxoethyl)benzonitrile. MS m/z: 164 (M+1)+.

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. filtrationThe mixture was filtered
  2. concentrationconcentrated
  3. dissolutionThe residue was dissolved in DCM
  4. dry with materialdried over anhydrous sodium sulfate
  5. custompurified by flash column chromatography

Sources & evidence

ORD record
ord-e6da56c1e0494bd09f771de800ef92c3
Source dataset
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09073882B2

Reaction notes

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