HCID 57444533, compound → 1-(3-Chlorophenyl)butane-1,3-dione
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][CH:20]=1)[C:5]([CH:7]([C:15](=[O:17])[CH3:16])C(OC(C)(C)C)=O)=[O:6]>FC(F)(F)C(O)=O>[Cl:1][C:2]1[CH:3]=[C:4]([C:5](=[O:6])[CH2:7][C:15](=[O:17])[CH3:16])[CH:18]=[CH:19][CH:20]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of tert-butyl 2-(3-chlorobenzoyl)-3-oxobutanoate (8.82 g) in trifluoroacetic acid (40 mL) was stirred for 1 hour under an ice-bath. The volatile was removed in vacuo, and the residue was partitioned between ethyl acetate (150 mL) and saturated sodium bicarbonate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated to give 1-(3-chlorophenyl)-1,3-butanedione as a pale orange crystal (533 g).
Workup
- customThe volatile was removed in vacuo
- customthe residue was partitioned between ethyl acetate (150 mL) and saturated sodium bicarbonate
- washThe organic layer was washed with brine
- dry with materialdried over magnesium sulfate
- customevaporated
Sources & evidence
- ORD record
- ord-1ec866a6824a4c478a1b4c6929dfaeb2
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07317009B2
Reaction notes
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