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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494886Generated: October 30, 2026

4-Bromothiophenol → 1-Bromo-4-[(2,2-diethoxyethyl)sulfanyl]benzene

https://huagongshe.com/reaction/494886

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromothiophenolHCID 66049—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product1-Bromo-4-[(2,2-diethoxyethyl)sulfanyl]benzeneHCID 1183367196.5%

Reaction Conditions

Temperature55 °C

Reaction Steps

1-Bromo-4-[(2,2-diethoxyethyl)thio]benzene (Chemical Abstracts number 96804-05-6) was prepared as described in Banfield et al.; J. Chem. Soc.; 1956; 2603-2607, and in Amin, et al.; J. Chem. Soc. Perkin Trans. 2; 1982; 1489-1492. 4-Bromothiophenol (20 g, 95%) in ethanol (80 mL) was treated with 21 wt % of sodium ethoxide in ethanol (36 g, 1.05 eq). The solution was heated at 55° C. for 30 minutes and bromoacetaldehyde diethylacetal (22.56 g, 1.05 eq) was added. The mixture was heated at reflux for 10 hours, ethanol was removed and the residue was diluted with 80 mL of water. The product was extracted with 2×120 mL of ethyl acetate. The combined ethyl acetate layer was washed with 2×40 mL of 15% NaCl and concentrated under vacuum to a brown oil (32.0 g, 92.5% potency, 96.5% yield). The product can be further purified by column chromatography (silica gel, 5:95 EtOAc:hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538138B2
Source datasetuspto-grants-2009_05
ORD IDord-a1e949ab39e14f5097e23a136b009c51
Source noteuspto-grants-2009_05