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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587783Generated: October 28, 2026

Triethylborane → 3-Chloro-5-ethylbenzaldehyde

https://huagongshe.com/reaction/587783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylboraneHCID 7357—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Bromo-5-chlorobenzaldehydeHCID 17750952—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-Chloro-5-ethylbenzaldehydeHCID 8408307842.9%

Reaction Steps

PdCl2(dppf)(37 mg, 0.046 mmol), potassium phosphate (1.93 g, 9.11 mmol) and triethylborane (1M in hexane, 0.45 g, 4.56 mmol) were added to a solution of 3-bromo-5-chloro-benzaldehyde (1.0 g, 4.56 mmol) in THF (20 mL) at ambient temperature and the mixture was refluxed for 12 h. The reaction mixture was brought to ambient temperature, diluted with EtOAc and washed with water. The organic layer was dried (Na2SO4), filtered, concentrated and the residue was purified by column chromatography on silica (100-200 mesh) eluting with 2% EtOAc in petroleum ether to afford the title compound (330 mg, 41%) as a pale yellow liquid: 1H NMR (400 MHz, DMSO-d6) δ 9.97 (s, 1H), 7.75 (d, J=1.6 Hz 1H), 7.73 (s, 1H), 7.65 (s, 1H), 2.74-2.68 (m, 2H), 1.23 (t, J=7.6 Hz, 3H); ESIMS m/z 168.0 ([M]+); IR (thin film) 3071, 1699, 692 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226501B2
Source datasetuspto-grants-2016_01
ORD IDord-cc58cae17ae949b88dd8aa6a8cb27bac
Source noteuspto-grants-2016_01