HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Formylbenzoic acid → 2,2,2-Trifluoro-1-methyl-1-(trifluoromethyl)ethyl 4-formylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1,1,1,3,3,3-Hexafluoro-2-methylpropan-2-ol | HCID 73936 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2,2-Trifluoro-1-methyl-1-(trifluoromethyl)ethyl 4-formylbenzoate | HCID 58930720 | — |
Reaction Steps
A mixture of 41.1 g (274 mmol) 4-carboxybenzaldehyde, 50 g (274 mmol) 1,1,1,3,3,3-hexafluoro-2-methyl-2-propanol, and 33.4 g (274 mmol) DMAP in 700 mL DCM was stirred until homogeneous (approximately 0.5 hr). The solution was cooled over an ice bath, under Ar, and 52.3 g (274 mmol) EDCI was added portion-wise. The reaction was stirred at RT for 48 hr. and concentrated to an oil on the rotovap. The oil was taken up with EA and washed with water, 2× with dil. Citric acid, 2× with dil. Sodium bicarbonate, and brine. The organic layer was dried over sodium sulfate and concentrated to 25.5 g pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932405B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-921c25c1f94041f09aa8ae1aa09b987f |
| Source note | uspto-grants-2011_04 |