HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741432Generated: October 31, 2026
1-(Bromomethyl)-3-phenoxybenzene → Ethyl 1-(p-chlorophenyl)-beta-oxo-alpha-(m-phenoxybenzyl)cyclopropanepropionate
https://huagongshe.com/reaction/1741432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(Bromomethyl)-3-phenoxybenzene | HCID 94544 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 1-(p-chlorophenyl)-beta-oxocyclopropanepropionate | HCID 21835800 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-(p-chlorophenyl)-beta-oxo-alpha-(m-phenoxybenzyl)cyclopropanepropionate | HCID 11070385 | 92% |
Reaction Steps
A mixture of sodium (0.31 g, 13.5 mmol) in ethanol (90 mL) is stirred at room temperature until the sodium dissolves. The resultant solution is heated to 70° C., treated dropwise with a solution of ethyl 1-(p-chlorophenyl)-β-oxocyclopropanepropionate (3.4 g, 12.8 mmol) in ethanol, stirred at 70° C. for one hour, treated dropwise with a solution of α-bromo-m-tolyl phenyl ether (4.0 g, 15.2 mmol) in ethanol, stirred at reflux overnight, stirred at room temperature for two days, and concentrated in vacuo to obtain a residue. A solution of the residue in ethyl acetate is washed sequentially with water, 10% sodium hydrogen carbonate solution and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo to obtain an oil. Chromatography of the oil using silica gel and a 19:1 hexanes/ethyl acetate solution gives the title product as a colorless oil (5.24 g, 92%) which is identified by NMR spectral analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05973190 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-386b673c226c4aec94b59ee7b4b8fc44 |
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| Source note | uspto-grants-1999_10 |
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