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ChemicalBook CAS DataBase List (2S)-2-(4-Bromo-phenyl)-morpholine-4-carboxylic acid tert-butyl ester
1131220-37-5

(2S)-2-(4-Bromo-phenyl)-morpholine-4-carboxylic acid tert-butyl ester synthesis

3synthesis methods
(2S)-2-(4-Bromo-phenyl)-morpholine

920798-90-9
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24424-99-5 Synthesis
Di-tert-butyl dicarbonate

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

(2S)-2-(4-Bromo-phenyl)-morpholine-4-carboxylic acid tert-butyl ester

1131220-37-5
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Yield:1131220-37-5 92%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in tetrahydrofuran at 20; for 17 h;

Steps:

208.b

b) (S)-tert-butyl 2-(4-bromophenyl)morpholine-4-carboxylate: (S)-2-(4-Bromo-phenyl)-morpholine (36.3 g, 150 mmol) and N,N-diisopropylethylamine (23.3 g, 31.4 ml, 180 mmol) in THF (360 ml) were treated with di-tert-butyl dicarbonate (39.3 g, 180 mmol). The reaction mixture was stirred for 17 h at rt, concentrated in vacuo, diluted with ethyl acetate, washed with 1 M-aq. citric acid (2 x 100 ml), dried over magnesium sulfate, filtered and concentrated in vacuo. The crude material was crystallized from hexane to afford 47.1 g (92%) (S)-tert-butyl 2-(4-bromophenyl)morpholine-4-carboxylate as an off-white solid. MS (ISP): 344.1 ([M+H]+).

References:

WO2011/76678,2011,A1 Location in patent:Page/Page column 124

(S)-2-(4-bromophenyl)morpholine  hydrochloride

1131220-34-2
9 suppliers
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24424-99-5 Synthesis
Di-tert-butyl dicarbonate

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

(2S)-2-(4-Bromo-phenyl)-morpholine-4-carboxylic acid tert-butyl ester

1131220-37-5
7 suppliers
inquiry