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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858786Generated: October 29, 2026

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

https://huagongshe.com/reaction/858786

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, 3 H), 2.00 (d, J=3.8 Hz, 1 H), 5.24 (m, 1 H), 7.19 (d, J=8.6 Hz, 1 H), 7.33 (dd, J=8.6, 2.5 Hz, 1 H), 7.75 (d, J=2.5 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-7ff39b8330664b8dbdc7e60ecc05b459
Source noteuspto-grants-2006_12