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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29473Generated: October 30, 2026

2-Bromopropane → Ethyl 5-bromo-3-methyl-4-[(propan-2-yl)oxy]-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/29473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 12542970—
SolventDimethylformamideHCID 6228—
ProductEthyl 5-bromo-3-methyl-4-[(propan-2-yl)oxy]-1-benzofuran-2-carboxylateHCID 53428887100%

Reaction Steps

To 0.50 g (1.7 mmole) of ethyl 5-bromo-4-hydroxy-3-methyl-1-benzofuran-2-carboxylate (Example 119, Step 1) in 7 mL DMF was added 0.51 g (3.75 mmole) of potassium carbonate and 0.48 mL (3 mmole) of 2-bromopropane and the reaction was stirred at room temperature overnight. The solvent was concentrated in vacuo, and the residue was extracted with ethyl acetate and water. The organic layer washed with water and brine, dried over sodium sulfate, filtered, and concentrated to provide 0.58 g of ethyl 5-bromo-4-isopropoxy-3-methyl-1-benzofuran-2-carboxylate. Yield: 100%; m.p. 48-50° C.; MS: 341.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-62a3dcf3a45e48b883368175bcb8307f
Source noteuspto-grants-2008_09