تفاعل #1107614

ord-bc22fc382ae84e2eb1f6ac1cead07909

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.STIRRINGstirred under a nitrogen atmosphere
  3. 3
    أخرىconsumed
  4. 4
    أخرىthe reaction was terminated
  5. 5
    workup.ADDITIONby adding H2O
  6. 6
    استخلاصextracted with CH2Cl2
  7. 7
    تجفيفThe separated organic layer was dried over MgSO4
  8. 8
    أخرىremoved the solvent under a reduced pressure
  9. 9
    أخرىThe residue thus obtained

الإجراء التجريبي

1.27 g of methyl 6-aminohexanoate hydrochloride (6.98 mmol) was dissolved in 25 ml of CH2Cl2 with stirring. 941 mg of triethylamine (9.3 mmol, 1.3 ml) was added to the mixture, and dicyclohexylcarbodiimide (DCC; 1.15 g, 5.58 mmol), dimethylaminopyridine (DMAP; 56.8 mg, 10 mol %), and 3-bromo-2-methylbenzoic acid (1.00 g, 4.65 mmol) was added thereto and stirred under a nitrogen atmosphere. After 24 hrs, the resulting mixture was subjected to thin layer chromatography to monitor the amount of the starting materials consumed, and the reaction was terminated by adding H2O thereto and extracted with CH2Cl2. The separated organic layer was dried over MgSO4 and removed the solvent under a reduced pressure. The residue thus obtained was subjected to a column chromatography (hexane:ethyl acetate=1:1, v/v) to obtain the title compound (497 mg, 31%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08716326B2uspto-grants-2014_05