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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668745Generated: October 26, 2026

Ammonium Chloride → (3-Bromo-5-ethoxy-phenyl)-(4-methoxy-3-methyl-phenyl)-methanone

https://huagongshe.com/reaction/1668745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-1-methoxy-2-methylbenzeneHCID 608315—
ReactantMagnesiumHCID 5462224—
Reactant3-bromo-5-ethoxy-N-methoxy-N-methylbenzamideHCID 57825192—
SolventTetrahydrofuranHCID 8028—
Product(3-Bromo-5-ethoxy-phenyl)-(4-methoxy-3-methyl-phenyl)-methanoneHCID 57825029—

Reaction Conditions

Temperature15 °C

Reaction Steps

A solution of 4-bromo-2-methylanisole (0.984 g, 4.9 mmol) in tetrahydrofuran (3 mL) was added dropwise to magnesium powder (0.127 g, 5.2 mmol) in tetrahydrofuran (1 mL) at room temperature. Under external heating the reaction mixture was brought up to reflux. After complete addition, reflux was maintained for 1 hour. Thereafter the mixture was cooled to 15° C., then diluted with tetrahydrofuran (1 mL) before a solution of 3-bromo-5-ethoxy-N-methoxy-N-methyl-benzamide (1.238 g, 4.3 mmol) in tetrahydrofuran (3 mL) was added dropwise. After complete addition, the mixture was heated to reflux for 1.5 hours. For the working-up, it was cooled to 5° C. and hydrolysed with a saturated solution of ammonium chloride (25 mL). The aqueous layer was extracted twice with ethyl acetate (2×50 mL), thereupon, the organic layers combined, washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The crude product was chromatographed on silica gel using a gradient of heptane/ethyl acetate=100/0 to 6/1 as the eluent. There were obtained 1.16 g (77% of theory) of the title compound as a colourless oil. Mass (calculated) C17H17BrO3 [348]; (found) [M+H]+=349, 351.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989449B2
Source datasetuspto-grants-2011_08
ORD IDord-1370c69d0d4c426b83d74bd31d111ff8
Source noteuspto-grants-2011_08