Reaktion #357718

Reaktionsgleichung

2-Nitrobenzyl alcohol

p-toluenesulfonyl chloride

→

22

Ausbeute 79.0%

2-nitrobenzyl tosylate

Ausbeute 79.0%

Lösungsmittel

triethylamine

DCM

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigebefore quenching with water
2. 2
   SonstigeThe organic layer was separated
3. 3
   Waschenwashed with 1 N HCl (1×50 ml), water (1×50 ml), 2 N NaOH (1×50 ml), water (1×50 ml) and brine (1×50 ml)
4. 4
   SonstigeThe organic layer was dried over anhydrous Na2 SO4
5. 5
   Einengenconcentrated under reduced pressure
6. 6
   Sonstigeto give a dull white solid, which
7. 7
   Sonstigewas further purified by flash chromatography (silica gel, dichloromethane/ethanol=9.5:0.5)

Vorschrift

2-Nitrobenzyl alcohol (1 g, 6.5 mmol) was dissolved in 40 ml of dry DCM and 1.36 ml of triethylamine. p-toluenesulfonyl chloride (1.24 g, 6.5 mmol) was added and the solution was stirred for 2 hours before quenching with water. The organic layer was separated and washed with 1 N HCl (1×50 ml), water (1×50 ml), 2 N NaOH (1×50 ml), water (1×50 ml) and brine (1×50 ml). The organic layer was dried over anhydrous Na2 SO4 and concentrated under reduced pressure to give a dull white solid, which was further purified by flash chromatography (silica gel, dichloromethane/ethanol=9.5:0.5) to give 2-nitrobenzyl tosylate, 22 (1.57 g, 79%). 1H-NMR (300 MHz, CDCl3) δ 8.08-7.99 (dd, J=9.21 & 8.04 Hz, 1H), 7.81 (d, J=8.4 Hz, 1H), 7.72-7.62 (m, 3H), 7.50 (d, J=8.85 Hz, 1H) 7.33 (d, J=8.43 Hz, 2H), 4.93 (s, 2H), 2.42 (s, 3H). 13C-NMR (60 MHz, CDCl3) δ 149.33, 146.12, 137.71, 135.27, 134.11, 133.09, 132.69, 132.57, 128.12, 123.89, 42.72, 20.64. MS (ESI): m/z 329.9 [(M+Na)]+.

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