تفاعل #1253202

ord-0027526028764d9993df4fc6455903f4

معادلة التفاعل

N=C(N)NCCC[C@H](N)C(=O)O
L-arginine
O=S(=O)(O)O
sulfuric acid
CCCCCCCCCCCCO
dodecanol
CCCCCCCCCCCCOC(=O)[C@@H](N)CCCNC(=N)N
arginine dodecyl ester
المردود 86.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
140°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىa clear light yellow solution resulted
  2. 2
    أخرىthe reaction
  3. 3
    غسيلwashed with water (3×25 ml)
  4. 4
    غسيلThe combined aqueous extracts were washed with diethyl ether (2×25 ml)
  5. 5
    أخرىprecipitated
  6. 6
    ترشيحFiltration of the suspension
  7. 7
    غسيلwashing of the filtrate with water (3× with 25 ml), acetone (3× with 25 ml) and diethyl ether (3× with 25 ml)

الإجراء التجريبي

A suspension of L-arginine free base (0.6 g, 3.5 mmol), sulfuric acid (0.31 ml, 7 mmol), and dodecanol (25 ml) were stirred together at 140° C. under nitrogen. After 6 hours, a clear light yellow solution resulted, and TLC indicated the reaction to be complete. The reaction mixture was diluted with diethyl ether (50 ml), and washed with water (3×25 ml). The combined aqueous extracts were washed with diethyl ether (2×25 ml), and basified with 1N KOH solution, upon which a white solid precipitated. Filtration of the suspension and washing of the filtrate with water (3× with 25 ml), acetone (3× with 25 ml) and diethyl ether (3× with 25 ml) gave arginine dodecyl ester. The yield was 86%. Melting point was 125-130° C. NMR gave the expected results for arginine dodecyl ester.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06613358B2uspto-grants-2003_09