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ChemicalBook CAS DataBase List 1-(4-IODOPHENYL)PIPERAZINE HYDROCHLORID&

1-(4-IODOPHENYL)PIPERAZINE HYDROCHLORID& synthesis

2synthesis methods
1-(4-IODOPHENYL)PIPERAZINE HYDROCHLORID&

624726-35-8
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$59.70/1g

24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
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$13.50/25G

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Yield:151978-66-4 92%

Reaction Conditions:

with sodium hydroxide in water at 20;

Steps:

22

To a solution of 4-iodophenylpiperazine hydrochloride (1.0 g, 3.08 mmol) in water (15 mL) was added sodium hydroxide (246 mg, 6.16 mmol), followed by di- tert-butyl dicarbonate (740 mg, 3.39 mmol). The reaction mixture stirred at room temperature overnight. The next day, the reaction mixture was filtered to collect tert- butyl 4-(4-iodophenyl)piperazine-l-carboxylate as a tan solid (1.1 g, 92% yield), which was washed with water (50 mL) and taken on to the next step without further purification. 1H NMR (600 MHz, CDCl3): δ 7.53 (d, 2H, J =9.0 Hz), 6.68 (d, 2H, J = 9.0 Hz), 3.57 (dd, 4H, J= 5.2, 5.0 Hz), 3.11 (dd, 4H, J= 4.9, 4.9 Hz), 1.49 (s, 9H); 13C NMR (150 MHz, CDCl3): δ 154.9, 151.1, 138.1, 118.8, 82.3, 80.2, 67.3, 49.2, 28.7; HRMS calcd for Ci5H21IN2O5: 389.07205 found 389.07165.

References:

WO2008/83056,2008,A2 Location in patent:Page/Page column 60