Phosphorus tribromide → 2-Bromomethyl-3-methylnaphthalene
Reaction equation
O[CH2:2][C:3]1[C:12]([CH3:13])=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=1.P(Br)(Br)[Br:15]>CCOCC>[Br:15][CH2:2][C:3]1[C:12]([CH3:13])=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a stirred solution of 2-hydroxymethyl-3-methylnaphthalene (2.47 g, 14.4 mmol) in dry Et2O (50 mL) cooled to 0° C. was added phosphorus tribromide (4.88 g, 18 mmol) dropwise over 20 minutes. The resulting heterogeneous mixture was stirred at 0° C. for 1.25 hours and then quenched with H2O (50 mL). The reaction mixture was diluted further with H2O (50 mL) and extracted with Et1O (2×150 mL). The combined organic layers were washed with H2O (1×100 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by filtration through silica gel using CH2Cl2 as eluent to give the product as an off-white solid (2.94 g, 87%).
Workup
- customquenched with H2O (50 mL)
- additionThe reaction mixture was diluted further with H2O (50 mL)
- extractionextracted with Et1O (2×150 mL)
- washThe combined organic layers were washed with H2O (1×100 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- filtrationThe residue was purified by filtration through silica gel
Sources & evidence
- ORD record
- ord-e3665f25a8c745bc8ecceaddb9d5c14c
- Source dataset
- uspto-grants-1990_01
- Patent number
- US04895861
Reaction notes
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