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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909591Generated: October 30, 2026

Dichloromethane → Methyl 2-(6-methoxy-1-benzofuran-3-yl)acetate

https://huagongshe.com/reaction/1909591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoron tribromideHCID 25134—
Reactant2-(6-Methoxy-1-benzofuran-3-yl)acetic acidHCID 736818—
ProductMethyl 2-(6-methoxy-1-benzofuran-3-yl)acetateHCID 1561871767%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598374B2
Source datasetuspto-grants-2013_12
ORD IDord-4bf9a0eb52fa4d8db77d4ab15a57601f
Source noteuspto-grants-2013_12