HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110222Generated: October 26, 2026
Sodium Iodide → Methyl 2-[(2-methoxy-2-oxoethyl)amino]acetate
https://huagongshe.com/reaction/1110222
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 5-amino-N,N'-didecyl-1,3-benzenedicarboxamide | HCID 19388948 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | Methyl 2-[(2-methoxy-2-oxoethyl)amino]acetate | HCID 428827 | — |
Reaction Steps
A mixture of 10.0 g (0.022 mol) of 5-amino-N,N'-didecyl-1,3-benzenedicarboxamide, 31 ml (0.33 mol) of methyl bromoacetate, 6.6 g (0.044 mol) of sodium iodide, 6.1 g (0.044 mol) of potassium carbonate and 0.32 g (0.001 mol) of tetrabutylammonium bromide in 100 ml of DMF was stirred and heated at 100° for 67 hours. The reaction mixture was concentrated on the oil pump and 100 ml of saturated NaHCO3 solution was added to the residue. The product was extracted with ethyl acetate and the extract was washed with 10% sodium bisulfite solution. The dried extract was concentrated at reduced pressure to an oil which was purified by HPLC using 35% ethyl acetate-toluene. The combined pure fractions were crystallized from methanol-water to give 8.2 g (63% yield, mp 71°-75°) of N-[3,5-bis[decylamino)carbonyl]phenyl]-N-(2-methoxy-2-oxoethyl)glycine methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05324747 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-9cdd9106293840598f5b4602ae9edcd7 |
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| Source note | uspto-grants-1994_06 |
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