HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Formylphenyl 4-(trifluoromethyl)benzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Formylphenyl 4-(trifluoromethyl)benzenesulfonate | HCID 22185671 | 52.3% |
Reaction Steps
A solution of 4-(trifluoromethyl)benzenesulphonyl chloride (2.4 g, 9.84 mmol) in pyridine (40 mL) is cooled to 0° C. Salicylaldehyde (1.44 g, 11.8 mmol) is added and stirred overnight. Water and ethyl acetate are added to the reaction and shaken. The organic layer is washed with dilute HCl (0.1 N×2), H2O, bicarbonate solution, H2O and dried with sodium sulfate. The organic layer is evaporated to dryness to give a yellow solid, which is recrystallized from ether/hexane to give 2-formylphenyl 4-(trifluoromethyl)benzenesulfonate as a yellow powder (1.70 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026339B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-fd21f148b6254d80a3e6df1b59f886b1 |
| Source note | uspto-grants-2006_04 |