Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603402Generated: October 29, 2026

1,3-Dibromopropane → 6-(3-Bromopropoxy)-3-methyl-1-benzofuran

https://huagongshe.com/reaction/603402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
Reactant3-Methyl-6-hydroxybenzofuranHCID 10855624—
SolventSodium HydroxideHCID 14798—
Product6-(3-Bromopropoxy)-3-methyl-1-benzofuranHCID 59300435169.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-methyl-1-benzofuran-6-ol (0.20 g, 1.35 mmol) in NaOH (6 M aqueous solution, 0.25 mL) was added 1,3-dibromopropane (0.48 mL, 0.46 mmol), and the mixture was heated at 80° C. for 2 h. The reaction mixture was cooled to rt, and NaOH (6 M aqueous solution, 0.11 mL) was added. The reaction mixture was heated at 80° C. for 1 h, cooled to rt, and partitioned between CH2Cl2 and NaHCO3 (saturated aqueous solution). The organic layer was dried, filtered, concentrated under reduced pressure, and purified by silica gel column chromatography (EtOAc/hexane (v/v)=1:19) to give 210 mg (58%) of the title compound containing minor impurities. This material was used in next step without further purification. 1H NMR (300 MHz, CDCl3): δ 7.38 (d, 1H), 7.32 (s, 1H), 7.0 (s, 1H), 6.88 (dd, 1H), 4.14 (t, 2H), 3.62 (t, 2H), 2.40-2.28 (m, 2H), 2.20 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906653B2
Source datasetuspto-grants-2011_03
ORD IDord-55ede39fffc949d2a9ab045104397a91
Source noteuspto-grants-2011_03