HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499671Generated: October 29, 2026
Triphenylphosphine → HCID 24694511, compound
https://huagongshe.com/reaction/499671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 68461234 | HCID 68461234 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Aluminum | HCID 5359268 | — |
| Product | HCID 24694511 | HCID 24694511 | 104.3% |
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-({[3-(methyloxy)phenyl]methyl}oxy)ethanol (114 mg, 0.626 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 (160 mg, title compound and impurity). The product was characterized by 1H NMR (400 MHz) in CDCl3. The purity of the compound was good enough to carry on the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767691B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-4f58443fee564a51a30adabf9f236dc3 |
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| Source note | uspto-grants-2010_08 |
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