Hydrochloric Acid → (2R)-1-methoxy-4-methyl-pentan-2-amine

HRID 1453421Notes

Reaction equation

HRID 1453421 reaction equation
[CH3:1][O:2][CH2:3][C@H:4]([N:9]1C(=O)C2C(=CC=CC=2)C1=O)[CH2:5][CH:6]([CH3:8])[CH3:7].O.NN.Cl>CO>[CH3:1][O:2][CH2:3][C@H:4]([NH2:9])[CH2:5][CH:6]([CH3:8])[CH3:7]

Participants

5

Conditions

Temperature
45 °C

Procedure

To a solution of (R)-2-(1-methoxy-4-methylpentan-2-yl)isoindoline-1,3-dione (example 9b) (3.87 g, 14.84 mmol) in methanol (30 mL), was added hydrazine hydrate (0.866 ml, 17.81 mmol) and the reaction mixture was warmed up to 45° C. for about 3 hours. The mixture was acidified with 2N HCl and stirred at 45° C. for 30 min. The solution was cooled to room temperature, filtered and evaporated. The residue was taken up with 2N NaOH and extracted with ether, dried over MgSO4, filtered and evaporated to give 1.51 g of (R)-1-methoxy-4-methylpentan-2-amine. Yield 77%. 1H NMR (500 MHz, CDCl3): δ 0.91 (m, 6H); 1.17 (m, 2H); 1.58 (s, 2H); 1.71 (m, 1H); 3.02 (m, 1H); 3.10 (m, 1H); 3.32 (m, 1H); 3.35 (s, 3H).

Workup

  1. temperatureThe solution was cooled to room temperature
  2. filtrationfiltered
  3. customevaporated
  4. extractionextracted with ether
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated

Sources & evidence

ORD record
ord-24ec10c18ec34672b414ed0f3bb96e32
Source dataset
uspto-grants-2009_01
Patent number
US07476399B2

Reaction notes

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