HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → Diazomethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Reactant | N-Methyl-N'-nitro-N-nitrosoguanidine | HCID 135436526 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Diazomethane | HCID 9550 | — |
| Product | HCID 53903884 | HCID 53903884 | — |
Reaction Steps
A solution of diazomethane is prepared from N-methyl-N'-nitro-N-nitroso guanidine (12.5 g), potassium hydroxide (50%, 20 ml), and ether (300 ml). TEA (7.7 ml) is added to the diazomethane solution (65%) followed by cyclohexane carboxylic acid chloride (7.4 ml) slowly at 0° . The reaction is stirred at 0° for 1 hr then for 18 hrs at 22° . A porecipitate forms, it is filtered and washed with ether, and the filtrate concentrated. The resulting oil is cooled to -78° , triturated with ether, then warmed to 22° and concentrated with reduced pressure and heat to give the title compound as an oil, NMR (acetone-d6) 5.4 and 1.4-0.8 δ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05220021 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-511508def6a047a6bd8e2f60f8f13887 |
| Source note | uspto-grants-1993_06 |