HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → 3,3,4,4,4-Pentafluorobutan-2-yl 4-formylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | 3,3,4,4,4-Pentafluorobutan-2-ol | HCID 78991 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,3,4,4,4-Pentafluorobutan-2-yl 4-formylbenzoate | HCID 58930722 | 67% |
Reaction Steps
A mixture of 4-carboxybenzaldehyde (21.9 g, 145.9 mmol), 3,3,4,4,4-pentafluoro-2-butanol (24.1 g, 146.9 mmol), EDC (33.5 g, 174.8 mmol) and DMAP (18.1 g, 148.1 mmol) was dissolved in DMF (60 ml) at rt. It was stirred for 36 h at rt. Hexane was added, it was washed with 1 N HCl, sat NaHCO3 and brine. The aqueous layers were extracted three times with hexane. It was dried over Na2SO4, filtered, concentrated, and the residue was purified by silica gel chromatography (ethyl acetate:hexane 1:10) to yield the desired aldehyde as a yellow oil (67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932405B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-0e95271d66ec49f88794be995e20835b |
| Source note | uspto-grants-2011_04 |