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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912017Generated: October 30, 2026

2,6-Dichlorobenzaldehyde → HCID 12105278, compound

https://huagongshe.com/reaction/912017

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorobenzaldehydeHCID 6737—
ReactantHCID 178420661HCID 178420661—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12105278HCID 12105278—

Reaction Steps

To a solution of 2,6-dichlorobenzaldehyde (880 mg, 5.03 mmol) in THF (10 mL) was added EtMgCl/THF (2.0 M, 3 mL, 6.0 mmol) at 0° C. under nitrogen, the resulting mixture was allowed to warm to rt and stirred at rt overnight. The mixture was quenched with sat. aq. NH4Cl (5 mL) at 0° C., then diluted with Et2O (50 mL), the organic phase was washed with brine (20 mL), and dried over anhydrous sodium sulfate. The residue was purified by silica gel chromatography (Hex:EtOAc=80:20) to give the title compound as a colorless oil. 1H NMR (CDCl3): δ=1.00 (t, J=7.4 Hz, 3H), 1.95-2.11 (m, 2H), 2.82 (d, J=10.4 Hz, 1H, —OH), 5.34 (m, 1H), 7.13 (t, J=7.6 Hz, 1H), 7.29 (d, J=7.8 Hz, 2H.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022206B2
Source datasetuspto-grants-2011_09
ORD IDord-cf42c01043ef41b59cbf4a8634ddf792
Source noteuspto-grants-2011_09