HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507684Generated: November 3, 2026
Sodium borohydride → 6-Methoxy-1-benzothiophene
https://huagongshe.com/reaction/507684
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Methoxybenzo[B]thiophen-3(2H)-one | HCID 12101625 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 6-Methoxy-1-benzothiophene | HCID 13634237 | 66.1% |
Reaction Steps
6-Methoxybenzo[b]thiophen-3(2H)-one (1.4 g, 7.76 mmol) was dissolved in a mixture of methanol (18 mL) and 2.5 M sodium hydroxide (3 mL). The mixture was treated with sodium borohydride (0.589 g, 15 mmol) in 10 mL of methanol and 3 mL of 2.5 M sodium hydroxide. The reflux was heated to reflux for 1 h and then at 60° C. overnight. The reaction was cooled down to room temperature and the methanol removed in vacuo. The remaining aqueous layer was acidified to pH 4 with 1 N hydrochloric acid. The aqueous layer was extracted with ethyl acetate and washed with 1 N HCl. The organic layer was further washed with water, saturated sodium bicarbonate, water and brine. The organic layer was dried with sodium sulfate, concentrated and purified by flash chromatography usng a gradient of 20 to 50% ethyl acetate in hexanes to afford a clear oil (0.843 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786132B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-79b1d4e6ffc8444688f13ea1be1bc5af |
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| Source note | uspto-grants-2010_08 |
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