HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-(4-chloro-2-nitrophenyl)-4-hydroxy-2-butynoate → Ethyl 4-(4-chloro-2-nitrophenyl)-4-oxo-2-butynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-(4-chloro-2-nitrophenyl)-4-hydroxy-2-butynoate | HCID 18358875 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-(4-chloro-2-nitrophenyl)-4-oxo-2-butynoate | HCID 18358889 | 51.3% |
Reaction Steps
To a solution of ethyl 4-(4-chloro-2-nitrophenyl)-4-hydroxy-2-butynoate(7.46 g, 26.3 mmoles) in dichloromethane (350 mL) cooled in an ice-bath was added manganese dioxide (26.2 g, 301.3 mmol). The reaction mixture was stirred for 20 minutes and then was allowed to warm to room temperature. The reaction mixture was stirred at room temperature for 130 minutes and then was filtered twice through a pad of CELITE™. The filtrate was purified by flash chromatography on silica gel (195 g), eluting with dichloromethane, to afford 3.80 g (51%) of the title compound as a brownish-orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313290B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-46f9017651ab4aa0b0dc26fa4db33aec |
| Source note | uspto-grants-2001_11 |