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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076552Generated: October 29, 2026

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

https://huagongshe.com/reaction/2076552

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 numberUS07923555B2
Source datasetuspto-grants-2011_04
ORD IDord-3b86dfdee85740b79402d4b2df2b99b7
Source noteuspto-grants-2011_04