Acetyl chloride → (R)-1-methoxy-4,4-dimethyl-1-oxopentan-3-aminium chloride

HRID 2171831Notes

Reaction equation

HRID 2171831 reaction equation
[NH2:1][C@@H:2]([C:7]([CH3:10])([CH3:9])[CH3:8])[CH2:3][C:4]([OH:6])=[O:5].[C:11]([Cl:14])(=O)C>CO>[Cl-:14].[CH3:11][O:5][C:4](=[O:6])[CH2:3][C@@H:2]([NH3+:1])[C:7]([CH3:10])([CH3:9])[CH3:8]

Participants

4

Conditions

Temperature
65 °C

Procedure

(R)-3-amino-4,4-dimethylpentanoic acid, 2a, was dissolved in methanol (1.4 L). The solution was cooled in an ice bath and acetyl chloride (67.0 mL, 947.0 mmol) was added dropwise (maintaining the temperature below 10° C.). The reaction mixture was heated to 65° C. and stirred at that temperature for 3 h. The reaction mixture was cooled to room temperature and then flushed with toluene to remove volatiles. The crude material was used without further purification: 1H NMR (400 MHz, MeOH-d4) δ 3.75 (s, 3H), 3.41 (t, 1H), 2.88 (dd, 1H), 2.64-2.46 (m, 1H), 1.04 (s, 9H).

Workup

  1. temperatureThe solution was cooled in an ice bath
  2. temperaturemaintaining the temperature below 10° C.)
  3. temperatureThe reaction mixture was cooled to room temperature
  4. customflushed with toluene
  5. customto remove volatiles
  6. customThe crude material was used without further purification

Sources & evidence

ORD record
ord-09e48850336e4b189079ccb823904d0f
Source dataset
uspto-grants-2015_06
Patent number
US09051319B2

Reaction notes

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