Hexane → HCID 67079158, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[C:6](Br)[CH:5]=[CH:4][C:3]=1[CH:9]([O:12][CH:13]([CH3:15])[CH3:14])[O:10][CH3:11].C([Li])CCC.CCCCCC.[Cl-].[NH4+]>C1(C)C=CC=CC=1.C(OC)(C)(C)C>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:9]([O:12][CH:13]([CH3:15])[CH3:14])[O:10][CH3:11]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Condition 4: Under a nitrogen atmosphere, 2,4-dibromo-1-(1-methoxy-1-methylethoxymethyl)benzene (500 mg, 1.48 mmol) was dissolved in toluene (3.65 ml) and t-butylmethyl ether (0.35 ml). To the solution was added dropwise n-butyllithium in hexane (1.6 M, 1.01 ml, 1.62 mmol) at 0° C. over 30 minutes. After completion of the addition, a saturated aqueous solution of ammonium chloride was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give a product containing 4-bromide and 2-bromide as an oil (373 mg). According to 1H-NMR analysis of the product, the ratio of 4-bromide:2-bromide was determined as 40:1, which was calculated based on the integration ratio of peaks of protons at benzyl position.
Workup
- additionAfter completion of the addition
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with a saturated aqueous solution of sodium chloride
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was evaporated under reduced pressure
- customto give a product
Sources & evidence
- ORD record
- ord-051815eea6ff4c05a22f7252b957cd5d
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09163051B2
Reaction notes
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