HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19763616, compound → HCID 19763623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19763616 | HCID 19763616 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19763623 | HCID 19763623 | — |
Reaction Steps
The oily residue obtained in stage a) is then heated in toluene (100 cc) and butanol (200 cc) in the presence of paratoluenesulphonic acid (0.5 g), with the separation of the water formed. After evaporating the reaction medium, the residue is chromatographed on a silica column (40:60 ethyl acetate/heptane eluant) to obtain a colourless oil (14.5 g) corresponding to a mixture of alcohol diastereoisomers, namely 2-(2,4-dichlorophenyl)-4-hydroxy-2-chloromethyltetrahydrofuran. This product is directly oxidized with chromic anhydride in acetic acid to obtain, after purification by silica column chromatography, furanone in the form of white crystals, m.p. 99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210198 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-93769233ea1a4b3db2046687f2096af4 |
| Source note | uspto-grants-1993_05 |