HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → 2-(4-Chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 2-Hydroxy-N-methylacetamide | HCID 223579 | — |
| Reactant | 2-(4-Chloro-2-methylphenoxy)acetaldehyde | HCID 12391459 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinone | HCID 12391493 | 11% |
Reaction Steps
4.6 g (0.0325 mole) of boron trifluoride etherate was added to a solution containing 4.6 g (0.025 mole) of (4-chloro-2-methylphenoxy)acetaldehyde and 2.5 g (0.028 mole) of N-methylglycolamide in 40 ml of tetrahydrofuran. After 24 hours at ambient temperature, the reaction mixture was concentrated under reduced pressure, extracted with ether, washed with water and dried. Purification by silica chromatography gave 0.7 g of 2-(4-chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinone as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062670 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-8691e936157a42a4bc5f2f957447cd70 |
| Source note | uspto-grants-1977_12 |