HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352284Generated: October 31, 2026
Water → Methyl 2-benzyloxycarbonylamino-5-oxo-2-tetrahydrofurancarboxylate
https://huagongshe.com/reaction/2352284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(((Benzyloxy)carbonyl)amino)-5-oxotetrahydrofuran-2-carboxylic acid | HCID 3106366 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-benzyloxycarbonylamino-5-oxo-2-tetrahydrofurancarboxylate | HCID 13995237 | 92.9% |
Reaction Steps
4.0 g sodium hydride (60% dispersion in mineral oil) was added to a solution of 27.93 g of 2-benzyloxycarbonylamino-5-oxo-2-tetrahydrofurancarboxylic acid obtained via the method described in the Journal of Organic Chemistry, 6, 878 (1941) in 100 ml dimethylformamide while stirring and ice-cooling the solution. 28.4 g methyl iodide was then added, and the reaction mixture was stirred at room temperature for 4 hours. 14.2 g methyl iodide was further added, and the mixture was stirred for 3 more hours. The mixture was poured into water and extracted with ethyl acetate. The organic layer was successively washed with aqueous sodium bicarbonate and brine, and thereafter it was dried (over MgSO4). The solvent was distilled off, and the precipitating crystal was collected by filtration and washed with ether to yield 27.25 g methyl 2-benzyloxycarbonylamino-5-oxo-2-tetrahydrofurancarboxylate in the form of a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04876251 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-c992b1045ccf4be79d62a1f04979c4cc |
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| Source note | uspto-grants-1989_10 |
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