Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Methyl 5-methoxy-1-benzofuran-2-carboxylate | HCID 14916651 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14916652 | HCID 14916652 | 95.4% |
Reaction Steps
Methyl 5-methoxybenzofuran-2-carboxylate (5.22 g, 25.3 mmol) was dissolved in dichloromethane, and sulfuryl chloride (3.76 g, 27.9 mmol) was added at such rate to maintain a temperature of 20° C. After stirring for 5 h the solution was dripped slowly onto ice water (70 mL). The organic phase was then washed with water, aqueous saturated NaHCO3 and again with water. The layers were separated and the organic portion was passed through a phase separation cartridge and evaporated to afford a solid (5.81 g), which was taken through to the next step with no further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796296B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-4d57552294e14a7aa8cfb6d036f38be2 |
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| Source note | uspto-grants-2014_08 |
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