HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 68505578, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 54215325 | HCID 54215325 | — |
| Reactant | Benzenecarbothioic acid, 2,5-difluoro-, hydrazide | HCID 55279024 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68505578 | HCID 68505578 | — |
Reaction Steps
To a solution of 3-(tert-butyldiphenylsilyloxy)-1-phenylpropan-1-one (1.98 g, 5.10 mmol) in 20 mL of a 3:1 mixture of EtOH:DCM was added 2,5-difluorobenzothiohydrazide (0.800 g, 4.25 mmol). The mixture was allowed to stir capped, at room temperature for 60 hours, then uncapped for 48 hours and then concentrated in vacuo. The residue was purified by flash column chromatography (Hexanes) to afford the desired product as an orange oil, 2.19 g, 92% which was contaminated with 3-(tert-butyldiphenylsilyloxy)-1-phenylpropan-1-one. The compound was carried forward to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580828B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-19038a76352c48d7841fa88ae26d6d04 |
| Source note | uspto-grants-2013_11 |