Reaktion #1610182

Reaktionsgleichung

4,5-diiodo-1,2-phenylene bis(trifluoromethanesulfonate)

Et3N

((pent-4-yn-1-yloxy)methyl)benzene

→

4,5-bis(5-(benzyloxy)pent-1-yn-1-yl)-1,2-phenylene bis(trifluoromethanesulfonate)

Ausbeute 79.5%

Lösungsmittel

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeA flame-dried 20 mL vial fitted with a screw-cap septa
2. 2
   SonstigeThe vessel was evacuated
3. 3
   Filtrationfiltered through a pad of silica
4. 4
   Einengenconcentrated in vacuo
5. 5
   SonstigePurification by flash chromatography (step gradient from Hex to 10% EtOAc/Hex)

Vorschrift

A flame-dried 20 mL vial fitted with a screw-cap septa was charged with Pd(PPh3)2Cl2 (0.06 equiv., 0.12 mmol, 84 mg), Cut (0.12 equiv., 0.24 mmol, 45.6 mg), and 4,5-diiodo-1,2-phenylene bis(trifluoromethanesulfonate) (1 equiv., 2 mmol, 1.25 g). The vessel was evacuated and backfilled with nitrogen (3×), followed by the sequential addition of THF (4 mL), Et3N (3 equiv., 6 mmol, 0.85 mL), and ((pent-4-yn-1-yloxy)methyl)benzene (2.3 equiv., 4.6 mmol, 802 mg) in THF (1 mL). The reaction was stirred for 3 h at rt, filtered through a pad of silica and concentrated in vacuo. Purification by flash chromatography (step gradient from Hex to 10% EtOAc/Hex) afforded 4,5-bis(5-(benzyloxy)pent-1-yn-1-yl)-1,2-phenylene bis(trifluoromethanesulfonate) (1.14 g, 1.59 mmol, 79%). TLC Rf=0.27 (10% EtOAc/Hex); 1HNMR (600 MHz): δ 7.42 (s, 2H), 7.27-7.39 (10H), 4.56 (s, 4H), 3.65 (t, 4H, J=6.0 Hz), 2.62 (t, 4H, J=7.1 Hz), 1.92-1.98 (m, 4H); 13CNMR (150 MHz): δ 138.8, 138.3, 128.4, 128.2, 127.59, 127.56, 126.3, 121.7, 119.6, 117.5, 115.3, 98.1, 77.4, 73.0, 68.5, 28.6, 16.5; FTIR: 2859, 2230, 1489, 1433, 1210, 1178, 1135, 1080, 732 cm−1; HRMS-ESI: calc. for C32H28F6O8S2Na (M+Na)+: 741.1027. found: 741.1039.

Quelle