HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920528Generated: October 26, 2026
Trimethylsilyl triflate → 1-[4-(Benzyloxy)-3-methylphenyl]-2-bromoethanone
https://huagongshe.com/reaction/920528
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]- | HCID 12969325 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[4-(Benzyloxy)-3-methylphenyl]-2-bromoethanone | HCID 12969327 | 70.2% |
Reaction Steps
To a solution of 1-(4-benzyloxy-3-methyl-phenyl)-ethanone (12.89 g; 53.1 mmol) in CH2Cl2 was added, dropwise, at 0° C., DIPEA (10.9 mL; 63.7 mmol) and trimethylsilyl trifluoromethanesulfonate (11.1 mL; 61.1 mmol). The resulting mixture was stirred at 0° C. for 1 hour, and subsequently, NBS (10.87 g; 61.1 mmol) was added in one portion. The mixture was allowed to warm to RT stirred overnight. Then the mixture was concentrated in vacuo, the residue dissolved in EtOAc, washed with water twice, and brine, dried (MgSO4), filtered, and concentrated in vacuo to afford 1-(4-benzyloxy-3-methyl-phenyl)-2-bromo-ethanone (11.90 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273017B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-fe1b9589b55747c4ba87726a178f5938 |
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| Source note | uspto-grants-2016_03 |
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