HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → Ethyl 2,2-difluoro-3-(4-methoxyphenyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 22345534 | HCID 22345534 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2,2-difluoro-3-(4-methoxyphenyl)propanoate | HCID 15487039 | 76.4% |
Reaction Steps
A solution of ethyl 2,2-difluoro-3-iodo-3-(4-methoxyphenyl)-propionate (5.24 g, 14.2 mmol) in toluene (125 ml) was treated with tributyltin hydride (28.9 g, 0.10 mol) and a few crystals of 2,2′-azobisisobutyronitrile. The resulting solution was then irradiated for 15 minutes at 25° C. with a sun lamp. The solvent was then evaporated in vacuo and the residue was partitioned between acetonitrile and pentane. The acetonitrile fraction was concentrated and chromatographed on silica gel (elution hexane-ethyl acetate, 85:15) to give 2.65 g (76%) of the title material as an oil: bp 90-95° C./0.1 torr (air bath temperature).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06924391B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-b984792602164982bf84865633fe0722 |
| Source note | uspto-grants-2005_08 |