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N-Iodosuccinimide → (4-Iodo-3-methylisoxazol-5-yl)acetic acid methyl ester

HRID 922243
Notes
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Reaction equation

HRID 922243 reaction equation
[CH3:1][C:2]1[CH:6]=[C:5]([CH2:7][C:8]([O:10][CH3:11])=[O:9])[O:4][N:3]=1.[I:12]N1C(=O)CCC1=O>FC(F)(F)C(O)=O>[I:12][C:6]1[C:2]([CH3:1])=[N:3][O:4][C:5]=1[CH2:7][C:8]([O:10][CH3:11])=[O:9]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 120273N-IodosuccinimideHCID 12366875Methyl 2-(3-methylisoxazol-5-yl)acetate

Product 1

HCID 66685715(4-Iodo-3-methylisoxazol-5-yl)acetic acid methyl esterYield 72.4%

Reagents, catalysts & solvents 1

HCID 6422Trifluoroacetic acidSolvent

Conditions

Temperature
65 °C

Procedure

To a sealed tube fitted with magnetic stirrer was charged methyl (3-methyl-1,2-oxazol-5-yl)acetate (0.9 g, 5.8 mmol) and N-iodosuccinimide (2.61 g, 11.6 mmol) in 10 mL trifluoroacetic acid. The reaction mixture was heated at 65° C. for 3 h. The RM was quenched with NaHCO3 solution (25 mL) and extracted with ethyl acetate (30 mL). The organic layer was washed with water (30 mL) and saturated brine solution (30 mL). The organic layer was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The product was obtained as brown solid (1.18 g, yield: 72.4%).

Workup

  1. customTo a sealed tube fitted with magnetic stirrer
  2. customThe RM was quenched with NaHCO3 solution (25 mL)
  3. extractionextracted with ethyl acetate (30 mL)
  4. washThe organic layer was washed with water (30 mL) and saturated brine solution (30 mL)
  5. dry with materialThe organic layer was dried over anhydrous Na2SO4
  6. customthe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-b802d6b9b7f54f6ba2613b59b6818ddd
Source dataset
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09278915B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes