تفاعل #2175464

ord-440299f454f14416bb5c56c767d4d92b

معادلة التفاعل

CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)O
N-Boc-(L)-Dopa
CCCC[N+](CCCC)(CCCC)CCCC.[OH-]
tetrabutylammonium hydroxide
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)[O-].CCCC[N+](CCCC)(CCCC)CCCC
title compound 1a
المردود 83.0%
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)c(O)c1)C(=O)[O-].CCCC[N+](CCCC)(CCCC)CCCC
(2S)-3-(3,4-Dihydroxyphenyl)-2-[(tert-butoxycarbonyl)amino]propanoic acid, tetrabutylammonium salt
المردود 83.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
4°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe mixture was then concentrated under reduced pressure
  2. 2
    أخرىdried
  3. 3
    أخرىby azeotroping twice with toluene
  4. 4
    أخرىThe residue was crystallized
  5. 5
    غسيلThe resulting crystalline solid was washed with acetone (400 mL×3)
  6. 6
    أخرىcollected on a Buchner funnel
  7. 7
    أخرىdried under high vacuum

الإجراء التجريبي

A solution of N-Boc-(L)-Dopa (175 g, 0.59 mol) in methanol (1 L) was cautiously mixed with a methanolic solution of tetrabutylammonium hydroxide (1.0 M, 0.55 L) at 0° C. for 30 min. The mixture was then concentrated under reduced pressure and dried by azeotroping twice with toluene. The residue was crystallized after cooling at 4° C. for 16 h. The resulting crystalline solid was washed with acetone (400 mL×3), collected on a Buchner funnel, and then dried under high vacuum to afford 245 g (83% yield) of the title compound 1a. 1H NMR (400 MHz, DMSO-d6): δ 0.94 (t, J=7.6 Hz, 12H), 1.30 (m, 17H), 1.60 (m, 8H), 3.18 (m, 8H), 4.58 (m, 1H), 5.68 (d, J=5.6 Hz, 1H), 6.30 (d, J=7.6 Hz, 1H), 6.46 (d, J=8.0 Hz, 1H), 6.51 (s, 1H), 8.85 (s, 1H): 8.94 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08435562B2uspto-grants-2013_05