HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445876Generated: October 27, 2026
Dichloromethane → Methyl 2-(6-methoxy-1-benzofuran-3-yl)acetate
https://huagongshe.com/reaction/445876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(6-Methoxy-1-benzofuran-3-yl)acetic acid | HCID 736818 | — |
| Product | Methyl 2-(6-methoxy-1-benzofuran-3-yl)acetate | HCID 15618717 | 67% |
Reaction Steps
To a solution of 2-(6-methoxybenzofuran-3-yl)acetic acid (0.6 g, 2.9 mmol) in anhydrous dichloromethane (20 mL) at −78° C. was added boron tribromide (1.5 eq.) The reaction was stirred at −78° C. for 30 minutes, 0° C. for 2 hours, and at room temperature overnight. The reaction mixture was cooled to 0° C. and quenched slowly with methanol. After stirring for 15 minutes a saturated sodium bicarbonate solution was added slowly to the mixture and allowed to stir at 0° C. for 30 minutes. Ethyl acetate was added and the layers were separated. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to give methyl 2-(6-methoxybenzofuran-3-yl)acetate (745) (67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476308B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-89e2b2c218c640b983eae893b0cefcc3 |
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| Source note | uspto-grants-2013_07 |
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