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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257783Generated: November 2, 2026

4-Methoxybenzenethiol → (2,2-Dimethoxyethyl)(4-methoxyphenyl)sulfane

https://huagongshe.com/reaction/1257783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzenethiolHCID 12765—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product(2,2-Dimethoxyethyl)(4-methoxyphenyl)sulfaneHCID 14175762100.4%

Reaction Steps

To an ice cooled solution of sodium ethoxide (3.26 g, 48.0 mmol) in ethanol (25.0 mL) was slowly added 4-methoxybenzenethiol (6.73 g, 48.0 mmol). The reaction mixture was stirred for 15 min. 2-Bromo-1,1-dimethoxyethane (5.64 mL, 48.0 mmol) was added, and the reaction mixture was refluxed for 2 h. After the precipitate was isolated by filtration, the mother liquor was evaporated under reduced pressure. The resultant residue was diluted with diethyl ether (100 mL) and washed with water and brine, dried over sodium sulfate, filtered, and concentrated to give the desired crude product (11.0 g) which was directly used in next step reaction without further purification. 1H-NMR (400 MHz, CDCl3): 7.40 (m, 2H), 6.85 (m, 2H), 4.47 (t, J=5.6 Hz, 1H), 3.80 (s, 3H), 3.34 (s, 6H), 3.01 (d, J=5.6 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461330B2
Source datasetuspto-grants-2013_06
ORD IDord-7acf733d785c42e5a28004d88fbdb33b
Source noteuspto-grants-2013_06