HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322235Generated: October 26, 2026
Triethylamine → Methyl 2-(3-methoxyphenylthiomethyl)-6-nitrobenzoate
https://huagongshe.com/reaction/322235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methoxybenzenethiol | HCID 84989 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 2-(bromomethyl)-6-nitrobenzoate | HCID 21708527 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(3-methoxyphenylthiomethyl)-6-nitrobenzoate | HCID 22009996 | 806.2% |
Reaction Steps
To a solution of 3-methoxythiophenol (0.54 g, 0.48 mmol) and triethylamine (0.43 ml, 0.59 mmol) in dichloromethane (30 ml) was slowly added methyl 2-bromomethyl-6-nitrobenzoate (1.45 g, 5.3 mmol) under ice-cooling, followed by stirring for 3 hours. After the reaction was completed, a saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture. The organic layer was washed successively with a saturated aqueous solution of sodium hydrogen carbonate and a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the organic layer was concentrated under reduced pressure. The obtained oily substance was purified by silica gel column chromatography (hexane/ethyl acetate=7/1) to give methyl 2-(3-methoxyphenylthiomethyl)-6-nitrobenzoate (1.29 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211227B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-c554047d9bd641eeb74d5597ade41352 |
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| Source note | uspto-grants-2001_04 |
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