HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783971Generated: October 29, 2026
Diethyl Carbonate → Ethyl benzo[b]thiophene-7-carboxylate
https://huagongshe.com/reaction/1783971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 7-Bromobenzo[b]thiophene | HCID 12045538 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl benzo[b]thiophene-7-carboxylate | HCID 49758023 | 71% |
Reaction Steps
7-bromobenzo[b]thiophene (500 mg, 2.36 mmol) is dissolved in dry THF (5.0 mL) under nitrogen. Magnesium turnings (530 mg, 2.83 mmol, 1.20 equiv.) are added and the resulting mixture is heated at reflux until dissolution of the magnesium has occurred. The resulting cloudy yellow solution is allowed to cool to rt and diethyl carbonate (2 mL, excess) is added and stirring continued for one hour, when ammonium chloride (10% aq) is added. The resulting mixture is partitioned between DCM and water and the aqueous layer is extracted with DCM. The organic fractions are combined, washed with brine, dried over Na2SO4 and adsorbed onto silica. Purification by LC using 8/2 cyclohexane/dichloromethane as the eluent afforded the title compound as a pale orange oil (346.2 mg, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501411B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-8557a574f6614ac88eef6422d26425a2 |
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| Source note | uspto-grants-2009_03 |
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