1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene → HCID 178440978, compound

HRID 2274726Notes

Reaction equation

HRID 2274726 reaction equation
[NH:1]1[C:5]2[CH:6]=[C:7]([C:10]3[O:14][C:13]([SH:15])=[N:12][N:11]=3)[CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.[C:16]([C:20]1[CH:27]=[CH:26][C:23]([CH2:24]Br)=[CH:22][CH:21]=1)([CH3:19])([CH3:18])[CH3:17]>CCO>[C:16]([C:20]1[CH:21]=[CH:22][C:23]([CH2:24][S:15][C:13]2[O:14][C:10]([C:7]3[CH:8]=[CH:9][C:4]4[NH:3][CH:2]=[N:1][C:5]=4[CH:6]=3)=[N:11][N:12]=2)=[CH:26][CH:27]=1)([CH3:19])([CH3:17])[CH3:18]

Participants

4

Reactant 2

HCID 878361-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 178527937HCID 178527937, compound

Product 1

HCID 178440978HCID 178440978, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

1 (0.33 g, 1.5 mmol), TEA (0.209 mL, 1.5 mmol) and 4-tert-butylbenzylbromide (0.292 mL, 1.5 mmol) were dissolved in 10 mL of EtOH and kept under reflux overnight. The solvent was removed and the remaining oil was purified by flash-chromatography on silica gel, applying a CHCl3/MeOH gradient.

Workup

  1. temperatureunder reflux overnight
  2. customThe solvent was removed
  3. customthe remaining oil was purified by flash-chromatography on silica gel

Sources & evidence

ORD record
ord-7dd7b347c5c24f43a02e7bf29e107968
Source dataset
uspto-grants-2015_09
Patent number
US09126987B2

Reaction notes

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