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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633542Generated: November 2, 2026

2-Bromoanisole → HCID 18507125, compound

https://huagongshe.com/reaction/1633542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanisoleHCID 11358—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18507125HCID 1850712581%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of magnesium (2.4 g, 100 mmmol), in THF (20 mL) at room temperature was added dropwise a solution of bromoanisole (9.1 mL, 71.4 mmol) in THF (30 mL). The reaction mixture was stirred at room temperature for 2 h and at 60° C. for 2 h. The mixture was cooled to room temperature and a solution of 4-bromobenzaldehyde (13.2 g, 71.4 mmol) was added over 5 min. The reaction mixture was stirred at room temperature for 3 h and was quenched by addition of aqueous saturated ammonium chloride (NH4Cl) (30 mL). The aqueous layer was washed with ether (3×40 mL), dried over Na2SO4 and concentrated. Purification by flash chromatography with hexanes/EtOAc (10:1) afforded 16.95 g of (4-bromo-phenyl)-(3-methoxy-phenyl)-methanol. 1HNMR (400 MHz, CDCl3) δ 7.46-7.41 (comp, 2H), 7.27-7.18 (comp, 3H), 6.91-6.87 (comp, 2H), 6.81-6.78 (m, 1H), 5.73 (s, 1H), 3.76 (s, 3H); MS (M+1) 294.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503905B1
Source datasetuspto-grants-2003_01
ORD IDord-cf9941b58d974d9b95fdba1c09593cc0
Source noteuspto-grants-2003_01