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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 1-(2-Bromoethyl)-4-methoxy-2-nitrobenzene | HCID 59353002 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methoxy-1-[2-(methylthio)ethyl]-2-nitrobenzene | HCID 59353021 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614215B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-0561b52d6756460d813ca35781699c94 |
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| Source note | uspto-grants-2013_12 |
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