Hydrochloric Acid → Methyl 2-chloroacetoacetate
Reaction equation
C[O-].[Na+].[Cl:4][C:5]1[C:6](=[O:14])[O:7][C:8](C)(C)[O:9][C:10]=1[CH3:11].Cl>CO>[CH3:8][O:7][C:6](=[O:14])[CH:5]([Cl:4])[C:10]([CH3:11])=[O:9]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 25% sodium methoxide in methanol (5 ml, 21.6 mmol) was added to a solution of 5-chloro-2,2,6-trimethyl-4H-1,3-dioxin-4-one (3.24 g, 18.4 mmol) in 10 ml of methanol at 20° C. The resulting yellow solution was stirred for 10 minutes, acidified with 10% HCl, and extracted with ether. Evaporation of the ether provided 2.35 g (94% yield, NMR assay ~90%) of a pale yellow oil, which was distilled to provide 1.8 g (66%) of pure title compound as a colorless liquid.
Workup
- extractionextracted with ether
- customEvaporation of the ether
- customprovided 2.35 g (94% yield, NMR assay ~90%) of a pale yellow oil, which
- distillationwas distilled
Sources & evidence
- ORD record
- ord-ec650cdb68064b0d844cbcb267cf0727
- Source dataset
- uspto-grants-1986_12
- Patent number
- US04633013
Reaction notes
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