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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432838Generated: October 26, 2026

3-Chlorothiophenol → 1-Chloro-3-[(2,2-dimethoxyethyl)sulfanyl]benzene

https://huagongshe.com/reaction/1432838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorothiophenolHCID 16257—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-3-[(2,2-dimethoxyethyl)sulfanyl]benzeneHCID 1817633695.8%

Reaction Steps

To a solution of 3-chlorothiophenol (2.4 g, 16.6 mmol) in THF (200 mL) at 0° C. is added bromoacetaldehyde dimethyl acetal (2.8 g, 16.6 mmol). To the solution is added sodium hydride (60% mineral oil dispersion, 0.70 g, 17.4 mmol). The reaction is stirred for 16 hours, and then is quenched by the addition of saturated NH4Cl (aq.). The solution is diluted with EtOAc. The organic layer is washed with a saturated NaCl (aq.). The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with hexanes. The title compound (3.7 g, 15.9 mmol) is obtained as an oil. 1H NMR (CDCl3, 300 MHz) δ7.32 (m, 1H), 7.25 (m, 1H), 7.12 (m, 1H), 4.47 (m, 1H), 3.07 (s, 3H), 3.02 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-202487eb3e4441d1beb7d77eade3d07a
Source noteuspto-grants-2009_11