HuagongsheHuagongshe Chemistry Print Report · For research reference only
Valeryl chloride → 2-(2-Pentanoyloxy-5-nitrophenyl)-1-(4-methoxyphenyl)-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | 2-(2-Hydroxy-5-nitrophenyl)-1-(4-methoxyphenyl)-ethanone potassium salt | HCID 66687980 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2-Pentanoyloxy-5-nitrophenyl)-1-(4-methoxyphenyl)-ethanone | HCID 66688801 | 98% |
Reaction Steps
4.23 g (35.0 mmol) of valeroyl chloride (compound of the formula VI) were added with cooling at −10° C. to 20° C. to a stirred suspension of 11.3 g (34.7 mmol) of 2-(2-hydroxy-5-nitrophenyl)-1-(4-methoxyphenyl)-ethanone potassium salt (example 1) in 50 ml of dry acetone. After 30 minutes the reaction was complete, as monitored by LC-MS, and the mixture was filtered through a layer of Celite to remove the precipitated potassium chloride. The solution was evaporated to dryness to give 9.23 g (98%) of a yellow oil which slowly crystallized while standing at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658808B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-835ecdb5ca6140f49b0b9dc67f9d4e95 |
| Source note | uspto-grants-2014_02 |