HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → (2-Trifluoromethyl-furan-3-yl)-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (2-Trifluoromethyl-furan-3-yl)-methanol | HCID 17953606 | — |
Reaction Steps
210 ml of chloroacetaldehyde were added over 30 minutes at 20° C. to 36.5 ml of ethyl 4,4,4-trifluoroacetoacetate in 600 ml of pyridine and the mixture was stirred for 52 hours. The reaction mixture was poured into 650 ml of concentrated hydrochloric acid and ice, stirred for 5 minutes and extracted with isopropyl ether. The extract was dried and the solvent was evaporated to obtain after chromatography on silica (eluent: 7/3 hexane/ethyl acetate), 43 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405865 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-9e1360cf4dc74a8d8fd4abed5b8dd2e1 |
| Source note | uspto-grants-1995_04 |