HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3-Bromo-2,5-difluoro-alpha-methylbenzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Bromo-2,5-difluorobenzaldehyde | HCID 14621021 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Bromo-2,5-difluoro-alpha-methylbenzenemethanol | HCID 14621022 | — |
Reaction Steps
To a stirred mixture of 13.3 g of 3-bromo-2,5-difluorobenzaldehyde and 300 mL of THF cooled to -35°/-20° under an N2 atmosphere is added 30 mL of 2.85M of MeMgBr in Et2O over 10 minutes. The cooling bath is removed and the mixture stirred 1 hour and finally poured into 1 L of ice/H2O. 10% HCl is added to bring the pH to ~2 and the mixture extracted with 3×200 ml of CH2Cl2. The CH2Cl2 extracts are washed with H2O, saturated NaHCO3, H2O (250 mL each) and stripped to furnish 14.5 g of crude 3-bromo-2,5-difluoro-α-methylbenzyl alcohol. M+1 ions are observed at 236 and 238 in the mass spectrum. The crude material is used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863959 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-66acacaa37294dea9887a62028044a39 |
| Source note | uspto-grants-1989_09 |