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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430420Generated: November 3, 2026

Iodoethane → HCID 67954059, compound

https://huagongshe.com/reaction/1430420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantDimethylacetamideHCID 31374—
ReactantHCID 67954075HCID 67954075—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 67954059HCID 67954059100%

Reaction Steps

60% sodium hydride (0.37 g, 8.5 mmol) was added to a N,N-dimethylacetamide (12.5 mL) solution of 6-benzyloxy-1,3,3-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione (2.5 g, 7.7 mmol) under ice cooling, and the mixture was stirred for 30 minutes. Ethyl iodide (0.68 mL, 8.5 mmol) was added dropwise thereto, followed by stirring at 10-20° C. for 2 hours. Water (17.5 mL) was added to the reaction solution, and ethyl acetate (20 mL) was added, followed by ethyl acetate extraction. The resulting organic layer was washed with water, and the solvent was distilled off. An aqueous solution of 70% methanol was added to the resulting residue, and the mixture was heated under reflux for 1 hour, followed by stirring for 30 minutes under ice cooling. Crystals were collected by filtration, then washed with an aqueous solution of 70% methanol, and dried at 60° C., thereby obtaining 2.71 g of a white, powdery target compound (yield: 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940889B2
Source datasetuspto-grants-2015_01
ORD IDord-380b802dbc1c4d67b2bf1028c5e226cb
Source noteuspto-grants-2015_01