Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607182Generated: October 30, 2026

Tetrahydrofuran → 3-Bromo-2,5-difluoro-alpha-methylbenzenemethanol

https://huagongshe.com/reaction/1607182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-Bromo-2,5-difluorobenzaldehydeHCID 14621021—
ReactantHCID 178418689HCID 178418689—
SolventDiethyl EtherHCID 3283—
Product3-Bromo-2,5-difluoro-alpha-methylbenzenemethanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863959
Source datasetuspto-grants-1989_09
ORD IDord-66acacaa37294dea9887a62028044a39
Source noteuspto-grants-1989_09