HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669526Generated: November 2, 2026
Triphenylphosphine → 1-(2-Bromoethoxy)-4-phenoxybenzene
https://huagongshe.com/reaction/1669526
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(4-Phenoxyphenoxy)ethanol | HCID 4676725 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Bromoethoxy)-4-phenoxybenzene | HCID 13254487 | 89.3% |
Reaction Steps
To a solution of 2-(4-Phenoxy-phenoxy)-ethanol (2.2 g, 9.55 mmol), triphenylphosphine (2.76 g, 10.5 mmol), and dichloromethane (DCM) (36.7 mL) after stirring at 0° C., was added N-Bromosuccinimide (1.87 g, 10.5 mmol). The resulting mixture was stirred at 0° C. for 30 minutes and then at room temperature for 30 minutes. Reaction mixture was concentrated in vacuo to obtain the crude mixture, which was purified by of silica gel flash chromatography, using EtOAc/hexane (gradient system), to obtain the product (2.5 g, 89%): 1H NMR (400 MHz, CDCL3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989480B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-56f60ac58aeb4eeab51af21fdc1c878e |
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| Source note | uspto-grants-2011_08 |
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