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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878917Generated: November 3, 2026

Potassium Carbonate → (2-Chlorophenyl)(2,2-diethoxyethyl)sulfane

https://huagongshe.com/reaction/1878917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
Reactanto-ChlorothiophenolHCID 80599—
SolventAcetoneHCID 180—
Product(2-Chlorophenyl)(2,2-diethoxyethyl)sulfaneHCID 5913310980%

Reaction Steps

To a solution of 2-chlorobenzenethiol (5.0 g, 34.5 mmol) in acetone (35 mL) was added 2-bromo-1,1-diethoxyethane (7.15 g, 36.3 mmol) followed by potassium carbonate (9.55 g, 69.1 mmol). The mixture was heated at reflux for 3 h. then cooled to rt, filtered and the filtrate evaporated under reduced pressure to yield the crude product. This material was purified by chromatography over silica gel eluting with ethyl acetate in hexanes (0→2%) to afford pure 1-chloro-2-(2,2-diethoxyethylsulfanyl)benzene (7.3, 80%). 1H NMR (400 MHz, CDCl3) δ=1.20 (t J=7.07 Hz, 6H), 3.15 (d, J=5.56 Hz, 2H), 3.51-3.61 (m, 2H), 3.63-3.74 (m, 2H), 4.69 (t, J=5.56 Hz, 1H), 7.12 (td, J=7.58, 1.52 Hz, 1H), 7.20 (td, J=7.58, 1.52 Hz, 1H), 7.36 (dd J=−7.83, 1.52 Hz, 1H), 7.39 (dd, J=8.08, 1.52 Hz, 1H); MS (ES+): m/z 187.17 [M-74].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314111B2
Source datasetuspto-grants-2012_11
ORD IDord-a732fa866f924803ae089e3085964547
Source noteuspto-grants-2012_11