Triethylamine → HCID 22253674, compound

HRID 1760282Notes

Reaction equation

HRID 1760282 reaction equation
[Br:1][CH:2]([CH3:12])[C:3]([NH:5][C:6]([CH3:11])([CH3:10])[C:7]([OH:9])=[O:8])=O.C(N(CC)CC)C.ClC(OCC)=O>CC(C)=O>[Br:1][CH:2]([C:3]1[O:8][C:7](=[O:9])[C:6]([CH3:11])([CH3:10])[N:5]=1)[CH3:12]

Participants

5

Procedure

To a stirring mixture of 2-(2-bromo-propionylamino)-2-methyl-propionic acid (50.0 g; 0.21 mol), triethylamine (23.37 g; 0.23 mol) and 150 mL acetone, cooled with an ice bath, was added a solution of ethyl chloroformate (25.07 g; 0.23 mol) in 40 mL acetone over a period of 10 minutes. The reaction mixture was then allowed to warm to room temperature and was stirred for 2 hours. The mixture was then filtered, and the solid was washed with 150 mL ether. The combined filtrate was concentrated under vacuum. Ether (100 mL) was added to the residue, and the mixture was filtered. After removal of the solvent under vacuum, the filtrate residue was distilled under reduced pressure (63-64° C.; 1 mmHg) to give 34.73 g (75%) of a colorless oil.

Workup

  1. temperaturecooled with an ice bath
  2. filtrationThe mixture was then filtered
  3. washthe solid was washed with 150 mL ether
  4. concentrationThe combined filtrate was concentrated under vacuum
  5. additionEther (100 mL) was added to the residue
  6. filtrationthe mixture was filtered
  7. customAfter removal of the solvent under vacuum
  8. distillationthe filtrate residue was distilled under reduced pressure (63-64° C.; 1 mmHg)

Sources & evidence

ORD record
ord-2d7357d8101b4524b6343449412d7e94
Source dataset
uspto-grants-2005_01
Patent number
US06841637B2

Reaction notes

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