HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → HCID 178503166, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4,4-Dimethyl-1,1-bis(methylsulfanyl)pent-1-en-3-one | HCID 2819743 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178503166 | HCID 178503166 | 48% |
Reaction Steps
Hydrazine hydrate (4 g, 3.9 ml) was added dropwise to a cooled solution of the product of Example 1 (15 g) in ethanol (75 ml). The reaction mixture was refluxed until evolution of methyl mercaptan ceased (2 hours), and allowed to cool. Most of the ethanol was evaporated off, and the residue was pitched into water, and ether extracted. The ethereal solution was dried over magnesium sulphate, and evaporated to give a pale yellow solid, which was recrystallised from 1:1 benzene/60°-80° petrol to give 3-t-butyl-5-(methylthio)pyrazole, 6.0 g, (48% yield), melting point 142°-4°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04331678 |
| Source dataset | uspto-grants-1982_05 |
| ORD ID | ord-8acb663a8ce4484d80e99e1a1e08e1c2 |
| Source note | uspto-grants-1982_05 |