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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627364Generated: November 3, 2026

3-Bromo-4-fluoro-α,α-dimethylbenzeneacetaldehyde → 3-Bromo-4-fluoro-α,β,β-trimethylbenzeneethanol

https://huagongshe.com/reaction/1627364

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-fluoro-α,α-dimethylbenzeneacetaldehydeHCID 86662253—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-4-fluoro-α,β,β-trimethylbenzeneethanolHCID 6674069466.1%

Reaction Steps

To a stirred solution of 2-(3-bromo-4-fluorophenyl)-2-methylpropanal (27 g, 110 mmol) in anhyd THF (300 mL) at 0° C. was added MeMgBr (3M in ether, 73 mL, 220 mmol, 2 eq) dropwise over 2 h. After stirring 1 h, the reaction was allowed to warm to room temperature, quenched carefully with 1N HCl and extracted with EtOAc. The combined extracts were washed with brine, dried over MgSO4 and evaporated in vacuo. The residue was purified by column chromatography (Hex/EA=10:1) to give 3-(3-bromo-4-fluorophenyl)-3-methylbutan-2-ol (19 g, 66%). 1H NMR (400 MHz, CDCl3) δ 7.56-7.54 (m, 1H), 7.32-7.28 (m, 1H), 7.07 (t, J=8.4 Hz, 1H), 3.84-3.79 (m, 1H), 1.31 (d, J=6.4 Hz, 6H), 1.04 (d, J=6.4 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785488B2
Source datasetuspto-grants-2014_07
ORD IDord-75001fa857b54b708c1832828066fe49
Source noteuspto-grants-2014_07