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N-(3-bromophenyl)-3-oxobutanamide → HCID 178429223, compound

HRID 279999
Notes
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Reaction equation

HRID 279999 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9](=[O:14])[CH2:10][C:11](=O)[CH3:12])[CH:5]=[CH:6][CH:7]=1>S(=O)(=O)(O)O>[OH:14][C:9]1[CH:10]=[C:11]([CH3:12])[C:5]2[C:4](=[CH:3][C:2]([Br:1])=[CH:7][CH:6]=2)[N:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 285615N-(3-bromophenyl)-3-oxobutanamide

Product 1

HCID 178429223HCID 178429223, compoundYield 84.3%

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Procedure

6.65 g (26.00 mM) of N-(3-bromophenyl)-3-oxobutyramide was heated in 30 mL of conc. sulfuric acid to 120° C. (oil bath temperature) for 1.5 h. The reaction mixture was then poured into ice, whereby precipitate was formed. This was filtered and washed repeatedly with water. After drying, it was recrystallised in 95% ethanol, providing 5.21 g (84%) of the product as a white solid: mp 275°-276° C.;

Workup

  1. additionThe reaction mixture was then poured into ice
  2. customwhereby precipitate was formed
  3. filtrationThis was filtered
  4. washwashed repeatedly with water
  5. customAfter drying
  6. customit was recrystallised in 95% ethanol

Sources & evidence

ORD record
ord-a0b98b5ab3084f38a9a26fd3520d5c65
Source dataset
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04587341

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes