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ChemicalBook CAS DataBase List Methyl trans-4-(tert-butoxycarbonylamino)cyclohexanecarboxylate
146307-51-9

Methyl trans-4-(tert-butoxycarbonylamino)cyclohexanecarboxylate synthesis

6synthesis methods
24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
846 suppliers
$13.50/25G

62456-15-9 Synthesis
trans-Methyl-4-aMinocyclohexanecarboxylate

62456-15-9
67 suppliers
$29.00/250mg

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Yield:146307-51-9 100%

Reaction Conditions:

with triethylamine in dichloromethane at 20; for 2.16667 h;Cooling with ice;

Steps:

3.1

Amine (132 g, 401 mmol) was suspended in dichloromethane (1000 ml) under ice-cooling. Triethylamine (123 ml, 882 mmol) and (Boc)2O (101 ml, 440 mmol) were sequentially added thereto and stirred for 10 minutes. After that, the mixture was stirred at room temperature for 2 hours and the solvent was removed. The residue was poured into aqueous citric acid (citric acid monohydrate 50 g in water 400 ml) to become pH4 and extracted with ethyl acetate. The organic layer was washed with water and dried over magnesium sulfate anhydrous. The solvent was removed under reduced pressure to quantitatively give the target compound.1H-NMR (DMSO-d6) δ ppm: 1.06-1.25 (m, 2H), 1.25-1.43 (m, 2H), 1.37 (s, 9H), 1.75-1.94 (m, 4H), 2.19 (tt, 1H, J=11.7, 3.9 Hz), 3.07-3.24 (m, 1H), 3.58 (s, 3H), 6.74 (d, 1H, J=6.6 Hz).

References:

US2010/273841,2010,A1 Location in patent:Page/Page column 21

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