HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949733Generated: October 26, 2026
Potassium Carbonate → 4,5-Dihydrobenzo[b]thieno[2,3-d]oxepine
https://huagongshe.com/reaction/1949733
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(2-(2-Iodophenoxy)ethyl)thiophene | HCID 64084785 | — |
| Catalyst | Tetraethylammonium Chloride | HCID 5946 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,5-Dihydrobenzo[b]thieno[2,3-d]oxepine | HCID 57900155 | — |
Reaction Steps
To a stirred solution of 2-iodophenol (6.7 g, 30.6 mmol), 2-(3-thienyl)ethanol (3.57 g, 27.8 mol) and triphenylphosphene (8.00 g, 30.6 mmol) in THF, was slowly added a solution of DEAD (4.8 ml, 30.6 mmol). Reaction mixture was stirred at room temperature for 3 hours. Purification on silica gave 3-[2-(2-iodo-phenoxy)-ethyl]-thiophene. A mixture of 3-[2-(2-iodo-phenoxy)-ethyl]-thiophene (1.55 g, 4.69 mmol), palladium(II) acetate (105 mg, 0.47 mmol), potassium carbonate (3.2 g, 23.45 mmol), triphenylphosphene (246 mg, 0.94 mmol) and tetraethylammonium chloride (1.3 g, 4.69 mmol) in DMF was microwaved at 100° C. for 1 hour. The reaction was diluted with dichloromethane and filtered through celite. The filtrate was washed with water, dried (MgSO4), and concentrated in-vacuo. Purification on silica gave 4,5-dihydrobenzo[b]thieno[2,3-d]oxepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399690B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-0d87de2083244ad3a4ff97cd98facd1b |
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| Source note | uspto-grants-2013_03 |
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