Réaction #66044

ord-10deba963c2b4ec3bb5960a884ad0927

Équation de réaction

C=CC[C@@H](N)C(=O)O
(2R)-2-amino-4-pentenoic acid
CO
methanol
O=S(Cl)Cl
thionyl chloride
C=CC[C@@H](N)C(=O)OC.Cl
title compound
Rendement 100.0%
C=CC[C@@H](N)C(=O)OC.Cl
Methyl (2R)-2-amino-4-pentenoate hydrochloride
Rendement 100.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrewas removed by evaporation
  2. 2
    Autrethe product crystallized with diethyl ether
  3. 3
    AutreThe diethyl ether was removed by evaporation

Mode opératoire

To a suspension of (2R)-2-amino-4-pentenoic acid (200 mg, 1.74 mmol) in methanol (6 mL) at 0° C. was added dropwise thionyl chloride (1 mL). The resulting solution was allowed to stir for 16 h before the solvent was removed by evaporation and the product crystallized with diethyl ether. The diethyl ether was removed by evaporation to yield the title compound (287 mg, 1.74 mmol, 100%) as a white solid which had spectral data in agreement with that reported.123 Mp 135-140° C. 1H NMR (CDCl3, 300 MHz): δ 8.70 (bs, 3H, NH3′); 5.89 (m, 1H, H4); 5.32 (d, J=17.3 Hz, 1H, H5a); 5.24 (d, J=10.1 Hz, 1H, H5b); 4.31 (m, 1H, H2); 3.81 (s, 3H, OCH3); 2.87 (t, J=6.3 Hz, 2H, H3). Mass Spectrum (ES, +ve) m/z 130 (100%) [M+]. HRMS calcd for C6H12NO2 130.0868, found 130.0870.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08524657B2uspto-grants-2013_09