HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → Ethyl 2-chloro-3-oxo-3-phenylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-chloro-3-oxo-3-phenylpropanoate | HCID 9855991 | — |
Reaction Steps
119.5 g of benzoyl acetic acid ethyl ester and 53.4 g of sodium acetate sicc. were dissolved in 1 l of glacial acetic acid and 100 ml of carbon tetrachloride at 40° C. A solution of 52 ml of sulphuryl chloride (density 1.67) in 50 ml of glacial acetic acid was added dropwise with vigorous stirring at 35°-40° C over a period of one hour. The reaction mixture was then stirred for one hour at 40° C and poured on about 10 l of water. The precipitated oily product was taken up with ethyl acetate and treated in the usual manner. 124 g of α-chlorobenzoylacetic acid ethyl ester were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04059447 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-6ab83a25b5984687b700ab27f15ebde5 |
| Source note | uspto-grants-1977_11 |