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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073832Generated: November 2, 2026

Ethyl Bromide → HCID 19887574, compound

https://huagongshe.com/reaction/1073832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19887580HCID 19887580—
SolventDimethylformamideHCID 6228—
ProductHCID 19887574HCID 19887574—

Reaction Steps

A solution of 1-benzyl-5-hydroxy-1-azoniabicyclo-[3.2.1]octane chloride (D7a, 3.05 g, 0.012 mole) in dry DMF (100 ml) under nitrogen was treated with sodium hydride (600 mg of 80% oil dispersion, 0.020 mole) and stirred at room temperature for 40 min. The mixture was then treated with bromoethane (4.7 ml, 0.063 mole) and stirred at room temperature for 16 h. The excess sodium hydride was destroyed by addition of ethanol (5 ml) and the mixture acidified with glacial acetic acid (5 ml) and then concentrated in vacuo to give an orange semi-solid containing the title compound (D8). This was used in the next step without any purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971975
Source datasetuspto-grants-1990_11
ORD IDord-3ccb4595dab844468a06447a7e4e0233
Source noteuspto-grants-1990_11