HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazinecarbothioamide, N-phenyl- → HCID 86743980, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazinecarbothioamide, N-phenyl- | HCID 730679 | — |
| Reactant | HCID 86743981 | HCID 86743981 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86743980 | HCID 86743980 | 114.3% |
Reaction Steps
To a mixture of 2R,4R, 5S)-4-formyl-5-[(Z)-6-methoxycarbonyl-2-hexenyl]-2-methyl-1,3-dioxane (62 mg) and 4-phenyl-3-thiosemicarbazide (46 mg) in ethanol (2 ml) was added acetic acid (1 drop) and the solution was stirred at room temperature for 4 hours. The mixture was diluted with chloroform (15 ml) and the solution was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo to give (2R,4R,5S)-5-[(Z)-6-methoxycarbonyl-2-hexenyl]-2-methyl-4-[4-(phenyl)thiosemicarbazonomethyl]-1,3-dioxane (110 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929639 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-5eefbcdf306d45b198f3dd66c6ebcd80 |
| Source note | uspto-grants-1990_05 |