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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798078Generated: November 3, 2026

N-bromobutanimide → [2-Bromo-3,5-bis(methoxymethoxy)phenyl]methanol

https://huagongshe.com/reaction/1798078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3,5-Bis(methoxymethoxy)benzylalcoholHCID 10443751—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product[2-Bromo-3,5-bis(methoxymethoxy)phenyl]methanolHCID 1095776883%

Reaction Steps

A solution of (3,5-bis-methoxymethoxy-phenyl)-methanol (9.16 g, 40.2 mmol) in DMF (40 mL) was treated with NBS (7.51 g, 42.2 mmol) at room temperature and the mixture was stirred at same temperature for 30 min. The residue was diluted with ethyl acetate and washed with brine. The organic phase was separated, dried (Na2SO4), and concentrated. The residue was purified by flash column chromatography (silica, hexanes/ethyl acetate=1:1) to afford the title compound (10.2 g, 83%). 1H NMR (300 MHz, CDCl3) δ 6.91 (s, 1H), 6.81 (s, 1H), 5.24 (s, 2H), 5.17 (s, 2H), 4.72 (d, J=6.3 Hz, 2H), 3.52 (s, 3H), 3.47 (s, 3H), 2.05 (t, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343944B2
Source datasetuspto-grants-2013_01
ORD IDord-661360b424bb463fbcd39e1ef42a0a26
Source noteuspto-grants-2013_01