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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromo-1-methoxy-2-methylbenzene | HCID 608315 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-bromo-5-ethoxy-N-methoxy-N-methylbenzamide | HCID 57825192 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Bromo-5-ethoxy-phenyl)-(4-methoxy-3-methyl-phenyl)-methanone | HCID 57825029 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989449B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-1370c69d0d4c426b83d74bd31d111ff8 |
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| Source note | uspto-grants-2011_08 |
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