Triethylamine → 2-Heptanoylaminopropionic acid

HRID 1814815

反応式

HRID 1814815 の反応式
Cl.C[O:3][C:4](=[O:8])[CH:5]([CH3:7])[NH2:6].C(N(CC)CC)C.[C:16](Cl)(=[O:23])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].[OH-].[Na+]>C(Cl)Cl.O>[C:16]([NH:6][CH:5]([CH3:7])[C:4]([OH:3])=[O:8])(=[O:23])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]

参加物

7

実験手順

30 g (291 mmol) of D,L-alanine methyl ester hydrochloride and 64.77 g (640 mmol) of triethylamine are initially charged in 300 ml of dry methylene chloride at 0° C. 43.24 g (291 mmol) of heptanoyl chloride in 50 ml of methylene chloride are added dropwise. The mixture is allowed to warm to RT and stirred at this temperature for 2 h. The precipitate is filtered off and the methylene chloride phase is extracted with saturated sodium bicarbonate solution and with saturated sodium chloride solution and dried over sodium sulfate. The solvent is removed under reduced pressure and the residue is dissolved in 300 ml of methanol. 300 ml of water, in which 46.55 g (1164 mmol) sodium hydroxide are dissolved, are added to this solution, and the mixture is stirred at RT for 2 h. The mixture is filtered, the methanol is evaporated using a rotary evaporator and the aqueous phase that remains is acidified to pH 1-2 using conc. Hcl. The precipitated product is filtered off and dried. Extraction of the aqueous phase with ethyl acetate gives a second product fraction.

後処理

  1. filtrationThe precipitate is filtered off
  2. extractionthe methylene chloride phase is extracted with saturated sodium bicarbonate solution and with saturated sodium chloride solution
  3. dry with materialdried over sodium sulfate
  4. customThe solvent is removed under reduced pressure
  5. dissolutionthe residue is dissolved in 300 ml of methanol
  6. additionare added to this solution
  7. stirringthe mixture is stirred at RT for 2 h
  8. filtrationThe mixture is filtered
  9. customthe methanol is evaporated
  10. customa rotary evaporator
  11. filtrationThe precipitated product is filtered off
  12. customdried
  13. extractionExtraction of the aqueous phase with ethyl acetate
  14. customgives a second product fraction

出典と根拠

ORDレコード
ord-a846dfed0a7b40e6993a4e847c372b7c
出典データセット
uspto-grants-2005_04
特許番号
US06878708B2

関連ノート

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