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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810265Generated: November 1, 2026

2-Bromo-5-(trifluoromethyl)benzaldehyde → 1-(2-Bromo-5-(trifluoromethyl)phenyl)ethanol

https://huagongshe.com/reaction/1810265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-(trifluoromethyl)benzaldehydeHCID 7018047—
ReactantHCID 178418373HCID 178418373—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Bromo-5-(trifluoromethyl)phenyl)ethanolHCID 57458795—

Reaction Steps

To 2-bromo-5-trifluoromethyl-benzaldehyde (1.0 g, 3.95 mmol) in THF (10 mL) at 0° C. under N2 was added methylmagnesium iodide (3M in diethyl ether; 2.6 mL, 7.91 mmol). The reaction was stirred for 2 hours, and then quenched with saturated aqueous NH4Cl and diluted with CH2Cl2. The aqueous layer was separated and extracted with CH2Cl2, and the combined organic layers were dried over MgSO4, filtered, and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362044B2
Source datasetuspto-grants-2013_01
ORD IDord-a00cfb1985bd46b297e0500e4f5c8c45
Source noteuspto-grants-2013_01