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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914699Generated: October 26, 2026

Sodium methanethiolate → 4-Methoxy-1-[2-(methylthio)ethyl]-2-nitrobenzene

https://huagongshe.com/reaction/1914699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant1-(2-Bromoethyl)-4-methoxy-2-nitrobenzeneHCID 59353002—
SolventEthanolHCID 702—
Product4-Methoxy-1-[2-(methylthio)ethyl]-2-nitrobenzeneHCID 5935302167%

Reaction Conditions

Temperature25.5 °C

Reaction Steps

A suspension of 1-(2-bromoethyl)-4-methoxy-2-nitrobenzene (14.7 g, 0.06 mol) in EtOH (150 mL) is stirred at 25-26° C. under a nitrogen atmosphere. Sodium thiomethoxide (7.9 g, 0.1 mol) is added in one portion at 25-26° C. and the reaction mixture is heated to reflux for 12 h. The solvent is removed under reduced pressure and the brown residue is taken up in cold water (100 mL). The crude product is extracted with EtOAc (2×200 mL). The organic layer is washed with water and brine (200 mL, each), then dried over Na2SO4 and the solvent is removed under reduced pressure to afford a brown oil. The crude product is purified by column chromatography (60-120 mesh silica gel, eluent 2% EtaAc in petrol ether) to give 8.3 g (67%) of the title compound as light brown liquid. 1H NMR (DMSO-d6, 400 MHz) δ 7.47-7.45 (m, 2H), 7.20-724(m 1H,), 3.81 (s, 3H), 3.01-2.97 (m, 2H), 2.69-2.66 (m, 2H), 2.05 (s, 3H). LC/MS: (ES+) 227.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614215B2
Source datasetuspto-grants-2013_12
ORD IDord-0561b52d6756460d813ca35781699c94
Source noteuspto-grants-2013_12