HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278787Generated: October 29, 2026
Triphenylphosphine → 4-Bromo-1-(bromomethyl)-2-methylbenzene
https://huagongshe.com/reaction/278787
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (4-Bromo-2-methylphenyl)methanol | HCID 22280088 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-1-(bromomethyl)-2-methylbenzene | HCID 22569018 | — |
Reaction Steps
A solution of (4-bromo-2-methyl-phenyl)-methanol (Intermediate 133, 319.0 mg, 1.58 mmol) and triphenylphosphine (466.0 mg, 1.74 mmol) in 5 mL CH2Cl2 was cooled to 0° C. and N-bromosuccinimide (309.0 mg, 1.74 mmol) was added in 5 portions over 20 minutes. The solution was warmed to 25° C. and stirred for 17 hours. The reaction was quenched by the addition of dilute aqueous NaHCO3. The resulting mixture was extracted with Et2O and the combined organic layers were washed with H2O and saturated aqueous NaCl before being dried (Na2SO4) and concentrated under reduced pressure. The title compound, 350.0 mg (84%), was isolated by column chromatography (2-3% EtOAc-hexanes) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06359135B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-7a210ad77d2e4119801efe2488364269 |
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| Source note | uspto-grants-2002_03 |
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