HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Diazomethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-Methyl-N'-nitro-N-nitrosoguanidine | HCID 135436526 | — |
| Reactant | HCID 178457149 | HCID 178457149 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Diazomethane | HCID 9550 | — |
| Product | HCID 178457148 | HCID 178457148 | — |
Reaction Steps
A solution of 20 mmol diazomethane was prepared by adding 4.29 g (29 mmol) 1-methyl-3-nitro-1-nitrosoguanidine to a 25% solution KOH (10 ml) and Et2O (30 ml) in an ice bath. The ethereal phase was decanted into a solution of 25 ml methanol containing 400 mg (1.28 mmol) of 2-di-n-propylamino-8-(5-hydroxypyrazol-3-yl)-1,2,3,4-tetrahydronaphthalene. The title compound was isolated by concentrating the reaction and purifying the 500 mg of brown oil crude by flash column chromatography eluting with 9:1 mixture of methylene chloride and methanol. 190 mg were collected. The correct mass of 328 was found using FAB spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05426226 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-32c1f651605248689d7f18aaa5e0f8c2 |
| Source note | uspto-grants-1995_06 |