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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68231Generated: October 29, 2026

Water → 4-{[(3-Chloro-4-hydroxyphenyl)thio]methyl}benzaldehyde

https://huagongshe.com/reaction/68231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-(Bromomethyl)benzaldehydeHCID 11206421—
Reactant2-Chloro-4-mercaptophenolHCID 14369743—
Solvent1,4-DioxaneHCID 31275—
Product4-{[(3-Chloro-4-hydroxyphenyl)thio]methyl}benzaldehydeHCID 5785981184%

Reaction Steps

Triethylamine (5.0 mL, 35.9 mmol) was added dropwise to a solution of 2-chloro-4-mercaptophenol (3.60 g, 22.4 mmol) and 4-bromomethyl benzaldehyde (3.93 g, 19.7 mmol) in dioxane (150 mL) at room temperature under nitrogen. The reaction mixture was stirred at room temperature for 20 hours. Water (100 mL) was added to the reaction mixture and it was then partitioned with ethyl acetate and brine (200 mL each). The aqueous layer was re-extracted with ethyl acetate (100 mL). The combined organic layers were dried over sodium sulphate and concentrated in vacuo affording a yellow solid. This was purified by trituration with acetonitrile (5 mL/g) for 30 minutes. After filtration this afforded a light yellow solid as the pure product, 84% yield, 5.27 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822439B2
Source datasetuspto-grants-2014_09
ORD IDord-baf0fbcee31e48baaab346ce0d70e562
Source noteuspto-grants-2014_09