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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296042Generated: November 1, 2026

Thionyl Chloride → 4-(4-Methyl-3-pyridylmethyl)benzaldehyde

https://huagongshe.com/reaction/2296042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-[(4-Methyl-3-pyridyl)hydroxymethyl]benzaldehyde diethylacetalHCID 20473415—
SolventBenzeneHCID 241—
Product4-(4-Methyl-3-pyridylmethyl)benzaldehydeHCID 1301897559.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 400 mg of the hydroxymethyl compound (prepared as described in Reference Example 4), 5 ml of benzene and 196 μl of thionyl chloride was stirred at 40° C. for one hour, and concentrated under reduced pressure. To the residue was added a saturated aqueous solution of sodium bicarbonate, and the mixture extracted with chloroform. The extract was washed with water, dried over magnesium sulphate and concentrated under reduced pressure. To the residue was added 5 ml of acetic acid and 175 mg of zinc powder, and the mixture stirred at room temperature for one hour, and then concentrated under reduced pressure. To the residue was added a saturated aqueous solution of sodium bicarbonate, and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulphate and concentrated under reduced pressure to give 166 mg of the title compound having the following physical characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04427682
Source datasetuspto-grants-1984_01
ORD IDord-120cdde665994fc1bbd130d99d5b6e31
Source noteuspto-grants-1984_01