Réaction #66045

Équation de réaction

51

Methyl (2R)-2-acetamido-3-(4-hydroxyphenyl)propanoate

K2CO3

allyl bromide

→

title compound

Rendement 85.4%

Methyl (2R)-2-acetamido-3-(4-allyloxyphenyl)propanoate

Rendement 85.4%

Solvants

DMF

Conditions de réaction

Traitement

1. 1
   AutreThe reaction was quenched with water (30 mL)
2. 2
   Extractionextracted with ethyl acetate (3×30 mL)
3. 3
   Lavagethe combined organics were washed with water (5×20 mL)
4. 4
   Autrebefore drying
5. 5
   AutreThe solvent was evaporated

Mode opératoire

To a solution of 51 (989 mg, 4.17 mmol), and anhydrous K2CO3 (1.15 g, 8.34 mmol) in DMF (10 mL) was added allyl bromide (1.01 g, 8.34 mmol) and the resulting mixture was allowed to stir for 16 h under a nitrogen atmosphere. The reaction was quenched with water (30 mL), extracted with ethyl acetate (3×30 mL), and the combined organics were washed with water (5×20 mL) before drying. The solvent was evaporated to yield the title compound (985 mg, 3.56 mmol, 85%) as a pale yellow solid. [α]D25-24.2 (c. 0.1, EtOH). Mp 90° C. 1H NMR (CDCl3, 300 MHz): δ 6.97 (d, J=8.7 Hz, 2H, ArH2′ and ArH6′); 6.80 (d, J=8.7 Hz, 2H, ArH3′ and ArH5′); 6.09 (d, J=7.8 Hz, 1H, NH); 6.01 (m, 1H, H2″); 5.37 (dd, J=1.8, 17.4 Hz, 1H, H3a″); 5.25 (dd, J=1.8, 10.5 Hz, 1H, H3b″); 4.80 (m, 1H, H2); 4.47 (d, J=5.5 Hz, 2H, H1″); 3.68 (s, 3H, OCH3); 3.04 (m, 2H, H3); 1.99 (s, 311, NCOCH3). Mass Spectrum (CI, +ve) m/z 278 (100%) [MH+]. HRMS (EI) calcd for C15H19NO4 277.131408, found 277.130309.

Source