HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → 2-(2,4-Dichlorophenoxymethyl)-4-thiazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 2-Mercaptoacetamide | HCID 12961 | — |
| Reactant | 2,4-Dichlorophenoxyacetaldehyde | HCID 5092937 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2,4-Dichlorophenoxymethyl)-4-thiazolidinone | HCID 12391494 | 20.1% |
Reaction Steps
To a solution containing 5.25 g (0.025 mole) of (2,4-dichlorophenoxy)acetaldehyde and 5.0 g (0.055 mole) of thioglycolamide in 100 ml of anhydrous ether was added 14.2 g (0.10 mole) of boron trifluoride etherate. The resulting solution was stirred at ambient temperature for 6 hours, washed with water, dried (MgSO4), and concentrated to dryness. The residual solid was purified by silica chromatography to give 1.4 g of 2-(2,4-dichlorophenoxymethyl)-4-thiazolidinone as a white crystalline solid melting at 134°-136°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062670 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-fc1b8f4a78604274aa0eaca870a4c7f8 |
| Source note | uspto-grants-1977_12 |