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KlementineJBS avatar KlementineJBS commented on June 9, 2024

04.05.22

1-bromoadamantane (103.6 mg, 0.482 mmol) was placed in a flask under nitrogen by solution transfer (MeCN, 5 mL). SnCl4 (0.14 mL, 1 M in heptane, 0.3 equiv.) and TMSN3 (0.15 mL, 1.14 mmol, 2.3 equiv.) were added and the reaction was left to reflux at 80 C from 1 pm.

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KlementineJBS avatar KlementineJBS commented on June 9, 2024

05.05.22

TLC at 11 am indicated reaction completion. Took an aliquot of crude reaction mixture to analyse via NMR.

TLC complete

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KlementineJBS avatar KlementineJBS commented on June 9, 2024

10.05.22

The reaction was quenched with water (15 mL) and then extracted with ethyl acetate (3 x 10 mL) and washed with brine (30 mL). After being dried over MgSO4, solvent was removed by rotary evaporation to give a crystalline yellowish solid.

Vial (empty): 15.8003 g
Vial (product): 15.8825 g
Product: 82.2 mg

crystalline solid

Image of solid obtained after rotary evaporation

NMR

NMR analysis seems to indicate some azidoadamantane present, though the peak at 2.15 is largely obscured by acetonitrile (peak at 2.17).

KBS11-6 crude_1.zip

KBS11-6 crude

KBS11-6 over KBS11-1

Reaction mixture (red) overlaid with known sample KBS 11-1 (blue)

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KlementineJBS avatar KlementineJBS commented on June 9, 2024

14.06.22

  1. Columned KBS11-6 but failed to find any product in fractions. (100% pet. benz. for 5 CV, 0 - 15% EtOAc in pet. benz. for 8 CV)

  2. Tried columning again and still saw no product. (25% EtOAc in pet. benz. for 10 CV)

Have retained column but unlikely to be able to recover much pure product.

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