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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-(((Benzyloxy)carbonyl)amino)-5-oxotetrahydrofuran-2-carboxylic acidHCID 3106366—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-benzyloxycarbonylamino-5-oxo-2-tetrahydrofurancarboxylateHCID 1399523792.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876251
Source datasetuspto-grants-1989_10
ORD IDord-c992b1045ccf4be79d62a1f04979c4cc
Source noteuspto-grants-1989_10