HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 3296813, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Naphthalenesulfonyl azide | HCID 10977355 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 3296813 | HCID 3296813 | 100% |
Reaction Steps
To a stirred solution of 24.52 grams (0.15 mole) of diethyl malonate and 34.0 grams (0.15 mole) of 2-naphthalenesulfonyl azide In 100 milliliters of acetonitrile was added 15.49 grams (0.15 mole) of triethylamine, dropwise, with cooling at 0° C.-5° C. On completing the feed the mixture was allowed to warm to room temperature while stirring for an approximate 16-hour period. Volatiles were stripped from the mixture under reduced pressure and the residue was slurried with ethyl ether and the inorganic salt filtered off. The filtrate was evaporated free of ether and purified by silica column chromatography to give 27.03 grams (0.15 mole) of diethyl diazomalonate as a yellow liquid. NMR analysis of the product indicated the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292937 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-f6f5edf40a6440f4a38ad0f858e82545 |
| Source note | uspto-grants-1994_03 |