HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 10975696, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 10964594 | HCID 10964594 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10975696 | HCID 10975696 | 99% |
Reaction Steps
A solution of 0.7M diazomethane in ether was slowly added to a solution of 6.0 g (42.8 mmol) of 5-oxocyclohex-2-ene-1-carboxylic acid in 100 mL of ether at 0 degrees centigrade, with swirling. The addition of diazomethane was continued until the bubbling ceased and a yellow color persisted. The solution was treated with a rapid stream of nitrogen until the yellow color was discharged. The solvent was removed by evaporation. Benzene (100 mL) was added and evaporated at room temperature using an aspirator. The residue was placed on a vacuum line for 2 hours to produce 6.5 g (42.4 mmol, 99 percent) of methyl 5-oxocyclohex-2-ene-1-carboxylate (oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05200513 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-8dc1a112e17f4398a2a21f8b5028150c |
| Source note | uspto-grants-1993_04 |