Triethylamine → HCID 66739176, compound

HRID 908062Notes

Reaction equation

HRID 908062 reaction equation
Cl.[C:2]([OH:7])(=[O:6])[CH2:3][CH2:4][CH3:5].[NH2:8][C@H:9]([C:20]([OH:22])=[O:21])[CH2:10][C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][CH:12]=1.C(N(CC)CC)C>ClCCl>[C:2]([OH:7])(=[O:6])[CH2:3][CH2:4][CH3:5].[NH2:8][C@H:9]([C:20]([OH:22])=[O:21])[CH2:10][C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][CH:12]=1

Participants

4

Reactant 2

HCID 8471TriethylamineHCID 66738995HCID 66738995, compound

Product 1

HCID 66739176HCID 66739176, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

1 g of tryptophane butanoate hydrochloride salt (commercially available from Sigma-Aldrich, St. Louis, Mo.) was suspended in 25 mL of dichloromethane and 600 μl of triethylamine was added to the suspension with stirring. Stirring was continued for 15 min and the resulting solution was transferred to a separatory funnel. The organic solution was washed twice with 25 mL of water followed by 25 mL of saturated aqueous sodium bicarbonate. The organic layer was then dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide tryptophane butanoate. The structure was confirmed using mass spectroscopy.

Workup

  1. stirringStirring
  2. customthe resulting solution was transferred to a separatory funnel
  3. washThe organic solution was washed twice with 25 mL of water
  4. dry with materialThe organic layer was then dried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-3c3871512ddc47cdbb7d2fc6aff7edd6
Source dataset
uspto-grants-2011_09
Patent number
US08017159B2

Reaction notes

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