HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Diethyl 1-benzyl-4-oxoazetidine-2,2-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 13505937 | HCID 13505937 | — |
| Solvent | Water | HCID 962 | — |
| Product | Diethyl 1-benzyl-4-oxoazetidine-2,2-dicarboxylate | HCID 13505935 | 75% |
Reaction Steps
34.1 g. (0.1 moles) of diethyl N-benzyl-N-(chloroacetyl)-amino-malonate prepared according to Example 19 and 18.2 ml. (13.2 g., 0.13 moles) of triethyl amine in 100 ml. of benzene are stirred at room temperature for 8 hours. The mixture is shaken with 100 ml. of water, 50 ml. of a 10% aqueous hydrochloric acid solution and again with 100 ml. of water. The organic phase is dried with magnesium sulfate, filtered and from the filtrate benzene is distilled off. The oily residue is distilled at 149° to 150° C., under a pressure of 0.1 mmHg. 23 g. (75%) of the named compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435322 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-e326b14dd8a44215accfb5ea883d9eb2 |
| Source note | uspto-grants-1984_03 |