HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-1,1,3,3,3-pentafluoro-2-propanone → 1,1,1,3,3-Pentafluoro-2-(4-ethoxyphenyl)-3-chloropropan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-1,1,3,3,3-pentafluoro-2-propanone | HCID 6601 | — |
| Reactant | Phenetole | HCID 7674 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1,1,1,3,3-Pentafluoro-2-(4-ethoxyphenyl)-3-chloropropan-2-ol | HCID 13880762 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of ethoxybenzene (67 g), chloropentafluoroacetone (100 g) and aluminium chloride (7 g) was charged to a Hastalloy lined cell at -78° C., the cell sealed and heated to 120° C. for 8 hours. After cooling and venting, the residue was taken up in chloroform and filtered through silica gel. After removal of the solvent by evaporation the residual solid was recrystallised from n-hexane to yield several crops of 1,1,1,3,3-pentafluoro-2-(4-ethoxyphenyl)-3-chloropropan-2-ol. (Total 70 g) mp. 84°-86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196610 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-a9168513170845018eb7c2abd7cbbd8e |
| Source note | uspto-grants-1993_03 |