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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670720Generated: October 31, 2026

Hydrochloric Acid → 2-Chloro-3-methoxybenzaldehyde

https://huagongshe.com/reaction/1670720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexachloroethaneHCID 6214—
Reactant3-MethoxybenzaldehydeHCID 11569—
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-3-methoxybenzaldehydeHCID 12575695—

Reaction Conditions

Temperature-70 °C

Reaction Steps

At 40° C. n-butyl lithium (6.25 mL, 1.6 M in hexane) was added to a solution of N,N,N′-trimethylethylenediamine (1.27 mL) in 10 mL tetrahydrofuran. After 15 min. the reaction mixture was cooled to −70° C. and a solution of 3-methoxybenzaldehyde (1.22 mL) in 5 mL of tetrahydrofuran was added. The reaction mixture was allowed to warm to 0° C. and was cooled again to −70° C. and n-butyl lithium (6.25 mL, 1.6 M in hexane) was added. The reaction mixture was allowed to warm to 10° C. and was cooled again to −30° C. before it was added to a solution of hexachloroethane (7.10 g) in 10 mL tetrahydrofuran. The reaction mixture was stirred for 2 h. at room temperature, poured into 20 mL 10% HCl in water and extracted several times with ethyl acetate. The combined organic phases were washed with saturated brine, dried on MgSO4 and concentrated. The title product was obtained after flash column chromatography (silica gel, heptane/ethyl acetate (75/25, v/v), Rf=0.38), followed by crystallisation from heptane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994189B2
Source datasetuspto-grants-2011_08
ORD IDord-e4b1b27124634e59b47a9fa6eab1a6cd
Source noteuspto-grants-2011_08