HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533877Generated: October 30, 2026
Triphenylphosphine → 2-{[(2-Bromoethyl)oxy]methyl}naphthalene
https://huagongshe.com/reaction/533877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-[(2-Naphthalenylmethyl)oxy]ethanol | HCID 59000353 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Aluminum | HCID 5359268 | — |
| Product | 2-{[(2-Bromoethyl)oxy]methyl}naphthalene | HCID 68960639 | 43.1% |
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 2-[(2-naphthalenylmethyl)oxy]ethanol (101 mg, 0.499 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 (57 mg, 43%). 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-e795d5842425472fb58fe84e4614751a |
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| Source note | uspto-grants-2014_10 |
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