HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 53703941, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 20348737 | HCID 20348737 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53703941 | HCID 53703941 | — |
Reaction Steps
A solution of 320 mgm (7.6 millimols) of diazomethane (prepared from 2.14 gm of p-toluenesulfonyl-methylnitrosoamide in 30 ml of ether and 0.4 gm of potassium hydroxide in 10 ml of 96% ethanol and subsequent distillation) was added, while stirring, to a suspension of 2.3 gm (7.5 millimols) of [1-(2'-fluoro-4-biphenylyl)-ethylsulfinyl]-acetic acid (m.p.: 164°-165° C.) in 20 ml of ether. The acid dissolved, accompanied by nitrogen evolution. After the reaction was finished, the mixture was evaporated, and the residue was recrystallized from benzene cyclohexane (1/5). Yield: 2.0 gm (83.5% of theory); m.p.: 75°-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04191776 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-14faa6a3bc1d4363ad7a4831f307724a |
| Source note | uspto-grants-1980_03 |