تفاعل #66047

ord-8e3d92c3d8c445248fa0cffae424e5ab

معادلة التفاعل

CC(=O)OC(C)=O
Acetic anhydride
COC(=O)[C@@H](N)Cc1ccc(I)cc1.Cl
93
COC(=O)[C@@H](N)Cc1ccc(I)cc1.Cl
Methyl (2S)-2-amino-3-(4-iodophenyl)propanoate hydrochloride
CC(=O)[O-].[Na+]
sodium acetate
COC(=O)[C@H](Cc1ccc(I)cc1)NC(C)=O
title compound
المردود 56.0%
COC(=O)[C@H](Cc1ccc(I)cc1)NC(C)=O
Methyl (2S)-2-acetamido-3-(4-iodophenyl)propanoate
المردود 56.0%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe resulting reaction
  2. 2
    ترشيحAfter 1 h the product was collected by vacuum filtration
  3. 3
    workup.DISSOLUTIONdissolved in ethyl acetate (30 mL)
  4. 4
    غسيلwashed with 2M sodium bicarbonate (2×30 mL)
  5. 5
    أخرىThe organic layer was dried
  6. 6
    أخرىevaporated

الإجراء التجريبي

To a solution of 93 (2.25 g, 6.80 mmol) in 10% HCl (10 mL) at 0° C. was added 4M sodium acetate (115 mL) and the resulting reaction was allowed to stir whilst equilibrating to 0° C. Acetic anhydride (50 mL) was added and the reaction allowed to proceed with vigorous stirring. After 1 h the product was collected by vacuum filtration, dissolved in ethyl acetate (30 mL) and washed with 2M sodium bicarbonate (2×30 mL). The organic layer was dried and evaporated to yield the title compound (1.31 g, 3.79 mmol, 56%) as a white solid. Mp 118-120° C. [α]D)27+93.8 (c. 0.1, CHCl3). 1H NMR (CDCl3, 300 MHz): δ 7.61 (d, J=8.4 Hz, 2H, ArH2′ and ArH6′); 6.84 (d, J=8.1 Hz, 2H, ArH3′ and ArH5′); 5.92 (d, J=7.2 Hz, 1H, NH); 4.87 (m, 1H, H2); 3.73 (s, 3H, OCH3); 3.11 (dd, J=6.0, 13.8, Hz, 1H, H3a); 3.03 (dd, J=5.4, 13.8 Hz, 1H, H3b); 1.99 (s, 3H, NCOCH3). Mass Spectrum (CI, +ve) m/z 348 (100%) [MH+]. HRMS calcd for C12H15NO3I 348.0097, found 348.0104.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524657B2uspto-grants-2013_09