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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295735Generated: October 31, 2026

3-Hydroxybenzaldehyde → 3-[(Methylsulfanyl)methoxy]benzaldehyde

https://huagongshe.com/reaction/1295735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantChloromethyl methyl sulfideHCID 16916—
SolventAcetoneHCID 180—
Product3-[(Methylsulfanyl)methoxy]benzaldehydeHCID 7141711236.31%

Reaction Steps

3-Hydroxybenzaldehyde (6.106 g, 50.00 mmol) was dissolved in acetone at room temperature. K2CO3 (13.821 g, 100.00 mmol), NaI (7.569 g, 50.00 mmol) and chloromethyl methyl sulfide (4.19 mL, 50.00 mmol) were added, and the mixture was allowed to stir for 80 h. The mixture was filtered, the filtrate concentrated to an oil, and the residue purified by SiO2 eluted with 99:1 CH2Cl2/MeOH to give 3.309 g (36.31%) of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244738B2
Source datasetuspto-grants-2007_07
ORD IDord-ab9bf3afdb284b5498c7c3dd59d15d9d
Source noteuspto-grants-2007_07