HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 2-(triphenyl-lambda5-phosphanylidene)acetate → 4,4-Difluoro-4-(4'-methoxy-biphenyl-4-yl)-butyric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 2-(triphenyl-lambda5-phosphanylidene)acetate | HCID 3862746 | — |
| Reactant | 4,4-Difluoro-4-(4'-methoxy-biphenyl-4-yl)-but-2-enoic acid ethyl ester | HCID 69784867 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4,4-Difluoro-4-(4'-methoxy-biphenyl-4-yl)-butyric Acid | HCID 9839508 | — |
Reaction Steps
4,4-Difluoro-4-(4′-methoxy-biphenyl-4-yl)-but-2-enoic acid ethyl ester. A solution of benzyl (triphenylphosphoranylidene)acetate (320 mg, 0.779 mmol) and 2,2-difluoro-2-(4′-methoxy-4-biphenyl)acetaldehyde (198 mg, 0.755 mmol) in toluene (4 mL) is heated to 90° C. with stirring for 2 hours. The reaction is cooled to room temperature and concentrated under reduced pressure. The crude product is purified by column chromatography (silica gel, 20% EtOAc/hexanes) to give the desired product as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852751B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-6f32d99f6e1f4661b04b1db88d46b76b |
| Source note | uspto-grants-2005_02 |