Water → 3-(2-Methylpropenyl)-benzylamine

HRID 2080132Notes

Reaction equation

HRID 2080132 reaction equation
[CH3:1][C:2]([CH3:12])=[CH:3][C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[C:7]#[N:8].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[CH3:1][C:2]([CH3:12])=[CH:3][C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[CH2:7][NH2:8]

Participants

6

Procedure

3-(2-Methylpropenyl)benzonitrile described in Preparation Example 136 (0.44 g, 2.8 mmol) was dissolved in tetrahydrofuran (5 mL), lithium aluminum hydride (0.16 g, 4.2 mmol) was added under stirring at room temperature, the solution was heated to 70° C., followed by stirring for 2 hours. The reaction solution was cooled on an ice bath, then, water (0.16 mL), an aqueous solution of 15% sodium hydroxide (0.16 mL) and water (0.48 mL) were sequentially added, then, the solid was filtered, and washed with tetrahydrofuran (10 mL). The filtrate and the washings were combined, and dried over anhydrous sodium sulfate. The solvent was evaporated in vacuo, and the title compound (0.40 g, 2.48 mmol, 88.7%) was obtained as a colorless oil.

Workup

  1. temperaturethe solution was heated to 70° C.
  2. stirringby stirring for 2 hours
  3. temperatureThe reaction solution was cooled on an ice bath
  4. filtrationthe solid was filtered
  5. washwashed with tetrahydrofuran (10 mL)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customThe solvent was evaporated in vacuo

Sources & evidence

ORD record
ord-27024e06c6c74af2aa1b67fc09de6870
Source dataset
uspto-grants-2011_04
Patent number
US07932272B2

Reaction notes

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