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 5.25g (0.025 mole) of (2,4-dichlorophenoxy)acetaldehyde and 5.0g (0.055 mole) of thioglycolamide in 100 ml of anhydrous ether was added 14.2g (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 1.4g 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 | US04090861 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-3f8a4448b3094ec4859c52174c3695e1 |
| Source note | uspto-grants-1978_05 |