Sarcosine → HCID 14129402, compound
Reaction equation
[NH:1]([CH2:3][C:4]([OH:6])=[O:5])[CH3:2].[C:7](Cl)(=[O:13])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]>[OH-].[Na+].CCOCC>[C:7]([N:1]([CH3:2])[CH2:3][C:4]([OH:6])=[O:5])(=[O:13])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Sarcosine (1.78 g, 20 mmol) was dissolved in 1N NaOH solution (40 ml) and Et2O (40 ml) was added. After cooling in an ice bath a solution of hexanoyl chloride (3.1 ml, 22 mmol) in Et2O (10 ml) was added dropwise. The mixture was stirred cold for 1 hour. The pH was then adjusted to about 8 by adding 1N NaOH solution (about 3 ml) and the mixture was stirred at room temperature 45 minutes. NaOH solution was added to about pH 9-10. The layers were separated and the aqueous layer was washed with Et2O (50 ml). After acidification of the aqueous layer with concentrated HCl and saturation with solid KCl, the product was extracted into CHCl3 (3×70 ml). The combined CHCl3 extracts were washed with saturated NaCl solution (25 ml), dried (MgSO4), and freed of solvent leaving the title compound as an oil (3.78 g, quant.) which was used without further purification.
Workup
- additionwas added dropwise
- stirringthe mixture was stirred at room temperature 45 minutes
- customThe layers were separated
- washthe aqueous layer was washed with Et2O (50 ml)
- extractionAfter acidification of the aqueous layer with concentrated HCl and saturation with solid KCl, the product was extracted into CHCl3 (3×70 ml)
- washThe combined CHCl3 extracts were washed with saturated NaCl solution (25 ml)
- dry with materialdried (MgSO4)
Sources & evidence
- ORD record
- ord-08e0a31eac904c33886674733d7daf72
- Source dataset
- uspto-grants-1988_04
- Patent number
- US04735962
Reaction notes
Loading…