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126026-17-3

Glycine, N-(2,2-dimethoxyethyl)-, ethyl ester synthesis

2synthesis methods
22483-09-6 Synthesis
Aminoacetaldehyde dimethyl acetal

22483-09-6
489 suppliers
$5.00/5g

Glycine, N-(2,2-dimethoxyethyl)-, ethyl ester

126026-17-3
2 suppliers
inquiry

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Yield: 71%

Reaction Conditions:

with potassium carbonate in N,N-dimethyl-formamide at 20;

Steps:

6.1 Step 1: ethyl 2-(2,2-dimethoxyethylamino)acetate
A mixture of 2,2-dimethoxyethanamine (5.0 g, 47.55 mmol), ethyl 2-bromoacetate (7.9 g, 47.30 mmol) and K2CO3 (6.64 g, 48.04 mmol) in DMF (40 mL) was stirred at room temperature overnight. Solvent was removed in vacuo, and the residue was purified by silica gel column (DCM:MeOH 20:1) to give the desired product ethyl 2-(2,2-dimethoxyethylamino)acetate as a colorless oil (6.5 g). Yield 71% (ESI 191.0 (M+H)+).

References:

Lazuli, Inc.;Harrison, Bryce A.;Bursavich, Matthew G.;Brewer, Mark;Gerasyuto, Aleksey I.;Hahn, Kristopher N.;Konze, Kyle D.;Lin, Fu-Yang;Lippa, Blaise S.;Lugovskoy, Alexey A.;Rogers, Bruce N.;Svensson, Mats A.;Troast, Dawn M. US2018/244648, 2018, A1 Location in patent:Paragraph 0227; 0228