HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)sulfur trifluoride → 4,4-Difluoro-4-(4'-methoxy-biphenyl-4-yl)-butyric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Ethyl α,α-difluoro-4′-methoxy[1,1′-biphenyl]-4-acetate | HCID 46220012 | — |
| Reactant | HCID 69784836 | HCID 69784836 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,4-Difluoro-4-(4'-methoxy-biphenyl-4-yl)-butyric Acid | HCID 9839508 | — |
Reaction Steps
Difluoro-(4′-methoxy-biphenyl-4-yl)-acetic acid ethyl ester. Diethylaminosulfur trifluoride (5 mL) is added directly to (4′-methoxy-biphenyl-4-yl)-oxo-acetic acid ethyl ester (3.77 g, 13.3 mmol), prepared as described by Neidlin, et. al., Arzneim.-Forsch. 1983, 33, 691-3. Dichloromethane (2 mL) is added and the mixture is stirred overnight at room temperature. The reaction is diluted with dichloromethane and slowly added to ice water. This mixture is extracted with ethyl acetate twice. The combined organic extracts are dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product is purified by column chromatography (silica gel, 5% EtOAc/hexanes) to give the desired product as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852751B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-e8ca589573444b1b96f7b6fcfff3247d |
| Source note | uspto-grants-2005_02 |