Réaction #1884983

Équation de réaction

isopropyl 2(S)-(tert-butoxycarbonylamino)-5-hydroxypentanoate

allyl methyl carbonate

BINAP

ether hexane

→

isopropyl 5-allyloxy-2(S)-(tert-butoxycarbonylamino)pentanoate

Solvants

ether

THF

Conditions de réaction

Traitement

1. 1
   Températurewas refluxed under nitrogen for 3 hours
2. 2
   Filtrationfiltered through celite
3. 3
   Autreevaporated
4. 4
   Autregiving a dark brown syrup

Mode opératoire

A degassed mixture of isopropyl 2(S)-(tert-butoxycarbonylamino)-5-hydroxypentanoate (product of step 26C, 17.6 g, 63.9 mmol), allyl methyl carbonate (24.0 ml, 213 mmol), Pd2(dba)3 (1.62 g, 1.78 mmol) and BINAP (4.42 g, 7.10 mmol) in THF (150 mL) was refluxed under nitrogen for 3 hours. After cooling to room temperature, the reaction was diluted with ether, filtered through celite and evaporated giving a dark brown syrup. Flash chromatography of the residue (silica gel, 30% ether/hexane) gave isopropyl 5-allyloxy-2(S)-(tert-butoxycarbonylamino)pentanoate as a viscous colorless oil, 16.3 g (81%): 1H NMR (300 MHz, Chloroform-D) δ 5.88 (ddt, 1 H, 17.4, 10.4, 5.5), 5.28 (m, 1 H), 5.22-5.11 (m, 1 H), 5.02 (sept., 1 H, J=6.2 Hz), 4.21 (br t, 1 H, J=6.7 Hz), 3.94 (dt, 2 H, J=5.9, 1.5 Hz), 3.42 (t, 2 H, J=5.9 Hz), 1.90-1.82 (m, 1 H), 1.75-1.57 (m, 3 H), 1.42 (s, 9 H), 1.21 (d, 3 H, J=6.2 Hz), 1.19 (d, 3 H, J=6.2 Hz). LCMS m/z 316 (M+H)+.

Source