HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710466Generated: October 25, 2026
Oxalyl chloride → 6-Methoxy-1-benzothiophene-2,3-dione
https://huagongshe.com/reaction/1710466
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Methoxybenzenethiol | HCID 84989 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Methoxy-1-benzothiophene-2,3-dione | HCID 3440848 | 47.4% |
Reaction Steps
To a solution of 3-methoxythiophenol (3.75 g, 26.7 mmol) in ether (20 mL) was added oxalyl chloride (3.7 mL, 43 mmol) dropwise. The mixture was heated at reflux for 1.5 h, cooled to rt, and concentrated in vacuo. The resulting yellow oil was dissolved in dichloromethane (50 mL), cooled to 0° C., and was treated with aluminum chloride (4.30 g, 32.0 mmol) in portions. The mixture was heated at reflux for 30 min, cooled to rt, and poured onto ice water with stirring. The organic layer was separated and successively washed with saturated, aqueous sodium bicarbonate, water, and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography (4/1 ethyl acetate/hexane) which provided 2.46 g (47%) of 6-methoxy-1-benzothiophene-2,3-dione as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790722B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-ea84e6025bfc44869b4bb1eac1393b9c |
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| Source note | uspto-grants-2010_09 |
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