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ChemicalBook CAS DataBase List N-Boc-4-oxo-L-Proline methyl ester
102195-80-2

N-Boc-4-oxo-L-Proline methyl ester synthesis

9synthesis methods
74844-91-0 Synthesis
N-Boc-trans-4-Hydroxy-L-proline methyl ester

74844-91-0
410 suppliers
$5.00/5g

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Yield:102195-80-2 98.17%

Reaction Conditions:

with 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical;trichloroisocyanuric acid in dichloromethane at 0 - 20; for 0.5 h;

Steps:

43.A Step A:
To a solution of N-Boc-trans-4-hydroxyl-L-methyl prolinate (114.00 g, 464.79 mmol) in dichloromethane (1.2 L) was added trichloroisocyanuric acid(113.42 g, 488.03 mmol) and then TEMPO (1.46 g, 9.30 mmol) was added at 0 °C.
After stirring for 0.5 h at 10-20 °C, the mixture was filtered with kieselguhr.
The dichloromethane phase was washed with sat. aq K2CO3 (1000 mL) twice, then with sat.aq NaCl (800 mL), dried over anhydrous Na2SO4, filtered and the filtrate was concentrated in vacuo to give N-Boc- 4-oxo-L-methyl prolinate (111.00 g, 456.30 mmol, 98.17%).
1H NMR (CDCl3, 400 MHz): δ 4.81-4.64 (m, 1H), 3.84 (d, J = 7.8 Hz, 2H), 3.73 (s, 3H), 2.99-2.84 (m, 1H), 2.55 (d, J = 20.0 Hz, 1H), 1.43 (d, J = 8.0 Hz, 9H).

References:

Medshine Discovery Inc.;SUN, Fei;DING, Charles Z.;CAI, Zhe;QIAN, Wenyuan;HU, Guoping;LI, Jian;CHEN, Shuhui EP3450430, 2019, A1 Location in patent:Paragraph 0272; 0273

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