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ChemicalBook CAS DataBase List N-Boc-L-tert-Leucine
62965-35-9

N-Boc-L-tert-Leucine synthesis

5synthesis methods
20859-02-3 Synthesis
L-tert-Leucine

20859-02-3
604 suppliers
$9.00/5G

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

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

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Yield:62965-35-9 100%

Reaction Conditions:

with triethylamine in methanol at 0 - 5;

Steps:

1.A STEP A; 2(S)-tert-Butoxycarbonylamino-3,3-dimethyl-butyric Acid

STEP A: 2(S)-tert-Butoxycarbonylamino-3,3-dimethyl-butyric Acid To a suspension of L-tert-leucine (26.1 g, 0.2 mol) in methanol (150 ML) was added triethylamine (56 ML, 0.4 mol) and the mixture cooled to 0° C. To the mixture was added slowly a solution of di-tert-butyldicarbamate (48 g, 0.22 mol) in methanol (40 ML) such that an internal temperature of between 0 and 5° C. was maintained.. The reaction was allowed to stir overnight and the solvents were removed in vacuo.. The residue was dissolved in ethyl acetate (200 ML) and washed with 10% w/v aqueous citric acid solution (3*100 ML).. The organic layer was dried over MgSO4, filtered and the solvents removed in vacuo to give the title product as a pale yellow oil (48.9 g, >100%, residual solvent). 1H NMR (CDCl3): δ/ppm 9.20 (1H, bs), 5.10 (1H, m), 4.15 (1H, m), 1.45 (9H, s), 1.00 (9H, s).

References:

US6716878,2004,B1 Location in patent:Page column 14

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