HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533870Generated: October 30, 2026
Triphenylphosphine → 1-(2-Bromo-ethoxymethyl)-4-chlorobenzene
https://huagongshe.com/reaction/533870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-[(4-Chlorobenzyl)oxy]-1-ethanol | HCID 2763751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Aluminum | HCID 5359268 | — |
| Product | 1-(2-Bromo-ethoxymethyl)-4-chlorobenzene | HCID 13654374 | 57% |
Reaction Steps
A solution of N-bromosuccinimide (272 mg, 1.53 mmol) in DCM (2.5 mL) was added to resin-bound triphenylphosphine (510 mg, 1.53 mEquiv, Fluka) in DCM (2.5 mL), and the reaction was stirred at rt for 10 min. A solution of 2-{[(4-chlorophenyl)methyl]oxy}ethanol (129 mg, 0.691 mmol) in DCM (1.5 mL) was added to the reaction, and the residual alcohol was transferred with additional DCM (1.5 mL). The reaction vial was capped, wrapped in aluminum foil, and stirred at rt for 20 h. The reaction was filtered through a SPE cartridge (5 g silica) eluting with the following 10 mL fractions: DCM (fraction 1), 30% EtOAc/hexanes (fraction 2), and 50% EtOAc/hexanes (fraction 3) to give the title compound (98 mg, 57%). The product was characterized by 1H NMR (400 MHz) in CDCl3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853404B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-da44829bc447435a83f4f386b9b9a026 |
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| Source note | uspto-grants-2014_10 |
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