HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533865Generated: October 29, 2026
Triphenylphosphine → 1-{[(2-Bromoethyl)oxy]methyl}-4-(1,1-dimethylethyl)benzene
https://huagongshe.com/reaction/533865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-({[4-(1,1-Dimethylethyl)phenyl]methyl}oxy)ethanol | HCID 10488591 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Aluminum | HCID 5359268 | — |
| Product | 1-{[(2-Bromoethyl)oxy]methyl}-4-(1,1-dimethylethyl)benzene | HCID 13654378 | 12% |
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-(1,1-dimethylethyl)phenyl]methyl}oxy)ethanol (160 mg, 0.768 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 (25 mg, 12%). The product was characterized by 1H NMR (400 MHz) in CDCl3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08853404B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-ec8e43886072402bad6d992109973d85 |
|---|
| Source note | uspto-grants-2014_10 |
|---|