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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046357Generated: November 1, 2026

3-Hydroxybenzaldehyde → 3-(2-Methylthioethoxy)benzaldehyde

https://huagongshe.com/reaction/1046357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
Reactant2-Chloroethyl methyl sulfideHCID 10965—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product3-(2-Methylthioethoxy)benzaldehydeHCID 23131712—

Reaction Steps

NaH (1.3 g, 54 mmol) is added to a solution of 5.0 g (41 mmol) 3-hydroxybenzaldehyde in 30 ml DMF at 0° C. After stirring for 1 h 4.44 ml (45 mmol) 2-chloroethyl methyl sulphide is added. The reaction mixture is warmed to room temperature and stirring is continued for 16 h. Then the reaction mixture is poured onto water and extracted with ethyl acetate. The combined organic layers are washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue is purified by flash-chromatography on silica gel (hexane/EtOAc=3:1) to afford the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569317B2
Source datasetuspto-grants-2013_10
ORD IDord-f0636b90a6a840eab4a176c3e2357644
Source noteuspto-grants-2013_10