HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → Ethyl 2-ethylidene-4-chloro-3-oxobutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Butanoic acid, 4-chloro-3-oxo- | HCID 119720 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-ethylidene-4-chloro-3-oxobutyrate | HCID 54518096 | — |
Reaction Steps
1 g of piperidine were dropped into a stirred mixture of 82 g of 4-chloroacetoacetic acid and 24 g of acetaldehyde at -20°. After stirring the mixture at -10° to -20° for 7 hours 100 ml of ethyl acetate were added and the solution was subsequently extracted three times with ice-cold 1 n hydrochloric acid and with water. The organic phase was dried over magnesium sulphate and concentrated. The oil which remained was subjected to Kugelrohr-distillation under a high vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04416880 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-c1952970ff0444f1beaa4929b2a3bb5b |
| Source note | uspto-grants-1983_11 |