HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795288Generated: November 2, 2026
Aminoacetaldehyde dimethyl acetal → [(2,2-Dimethoxy-ethylaminooxalyl)-amino]-acetic acid ethyl ester
https://huagongshe.com/reaction/1795288
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | Ethyl N-[ethoxy(oxo)acetyl]glycinate | HCID 2779372 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | [(2,2-Dimethoxy-ethylaminooxalyl)-amino]-acetic acid ethyl ester | HCID 9899933 | — |
Reaction Steps
To a solution of N-ethoxycarbonylmethyl-oxalamic acid ethyl ester (84.0 g, 414 mmol) 2–1 in 2-propanol (500 mL) was added aminoacetaldehyde dimethyl acetal (45.7 g, 435 mmol) in one portion. After stirring overnight at room temperature, the reaction mixture was concentrated to a thick orange oil. This thick slurry was diluted with 2-propanol (300 mL) and the solid was broken up with a spatula. Filtration afforded a solid which was further rinsed with an additional portion of 2-propanol. Removal of residual 2-propanol was accomplished via high vacuum to afford a light orange solid: 1H NMR (CDCl3) δ 7.82 (br s, 1H), 7.50 (br s, 1H), 4.41 (t, 1H, 5.3 Hz), 4.24 (q, 2H, 7.1 Hz), 4.09 (d, 2H, 5.9 Hz), 3.47 (dd, 2H, 5.3, 6.2 Hz), 3.40 (s, 6H), 1.30 (t, 3H, 7.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07026324B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-d5c0dd156c85473aa698d34d6063b136 |
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| Source note | uspto-grants-2006_04 |
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