HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus tribromide → 1-(Bromomethyl)-4-ethynylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | (4-Ethynylphenyl)methanol | HCID 11170993 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Bromomethyl)-4-ethynylbenzene | HCID 53426610 | — |
Reaction Steps
4-Ethynylbenzyl alcohol a (1 g, 7.57 mmol) was diluted in 20 ml DCM, and cooled to 0° in ice bath. Phosphorus tribromide (4.1 g, 15 mmol) was added dropwise. The reaction was allowed to warm to room temperature gradually, and stirred under nitrogen overnight. The reaction was quenched by addition of H2O in ice bath, extracted by DCM. Combined organic layers were washed with brine, dried over Na2SO4 and concentrated to dryness. The crude material was purified by chromatography (ISCO) using 100% hexane to give pure 4-ethynylbenzyl bromide b (220 mg). M+H+ 195.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08907092B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-ff95e10914264fe285f7be72a60264fe |
| Source note | uspto-grants-2014_12 |