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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453240Generated: November 1, 2026

5-Bromo-2-chlorobenzaldehyde → 1-(5-Bromo-2-chlorophenyl)ethanol

https://huagongshe.com/reaction/1453240

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-chlorobenzaldehydeHCID 10608925—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Bromo-2-chlorophenyl)ethanolHCID 5876264491%

Reaction Steps

Methyl lithium (11.6 mL, 16.3 mmol, 1.4M in ether) was added to a cooled −78° C. solution of 5-bromo-2-chloro-benzaldehyde (2.75 g, 12.5 mmol) dissolved in THF (40 mL). The reaction mixture was stirred for 15 hours and then quenched with saturated NH4Cl and extracted with EtOAc. The organic extracts were washed with 1N HCl, brine, dried over Na2SO4 and concentrated to an oil. The oil was purified by flash column chromatography (0% to 10% EtOAc in hexanes) to give the title compound as a solid (2.63 g, 91%). 1H NMR (400 MHz, CDCl3): δ 6.32 (d, J=6.3 Hz, 3H), 2.00 (d, J=3.8 Hz, 1H), 5.24 (m, 1H), 7.19 (d, J=8.6 Hz, 1H), 7.33 (dd, J=8.6, 2.5 Hz, 1H), 7.75 (d, J=2.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-90a8428f475e4b27806682400aa21d61
Source noteuspto-grants-2009_01