HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385708Generated: October 28, 2026
Acetone → 2-{3,5-Difluoro-4-[2-methoxyvinyl]phenyl}propan-2-ol
https://huagongshe.com/reaction/385708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(4-Bromo-2,6-difluorophenyl)vinyl methyl ether | HCID 67027625 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-{3,5-Difluoro-4-[2-methoxyvinyl]phenyl}propan-2-ol | HCID 67028878 | — |
Reaction Steps
To a cooled (−78° C.) solution of 2-(4-bromo-2,6-difluorophenyl)vinyl methyl ether (45 g, 0.18 mol) in methyl tert-butyl ether (300 mL) was added n-BuLi (75 mL of 2.5M in hexanes, 0.19 mol), and the mixture was stirred at −78° C. for one hour. A solution of acetone (13.6 g, 0.24 mol) in methyl tert-butyl ether (100 mL) was added dropwise to the reaction mixture and the resulting solution was stirred at −78° C. for two hours. Water (90 ml) was added to quench the reaction. The resulting biphasic mixture was extracted with ethyl acetate (2×). The organic layers were dried and concentrated in vacuo. Purification via flash chromatography afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08367706B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-1fa293a6fad04ebeaa21820e49e76a12 |
|---|
| Source note | uspto-grants-2013_02 |
|---|