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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636581Generated: October 31, 2026

Bromine → Ethyl 3-(7-bromo-2,3-dihydro-1-benzofuran-5-yl)propanoate

https://huagongshe.com/reaction/1636581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
ReactantEthyl 3-(2,3-dihydrobenzofuran-5-yl)propanoateHCID 11053175—
SolventAcetic AcidHCID 176—
ProductEthyl 3-(7-bromo-2,3-dihydro-1-benzofuran-5-yl)propanoateHCID 1089187897.5%

Reaction Steps

Bromine (10.5 g, 65.8 mmols) was dropwise added to an acetic acid (150 ml) solution containing ethyl 3-(2,3-dihydrobenzofuran-5-yl)propionate (14.5 g, 65.8 mmols) and sodium acetate (5.94 g, 72.4 mmols), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Water was added to the residue, which was then extracted with ethyl acetate. The extract was washed with a saturated saline solution and then dried with anhydrous magnesium sulfate. This was concentrated under reduced pressure to obtain 19.2 g (yield: 97%) of the target compound. This was oily.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034239
Source datasetuspto-grants-2000_03
ORD IDord-8a31fc9fbf8c4c2cb870f0201252d965
Source noteuspto-grants-2000_03