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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975691Generated: November 2, 2026

Iodoethane → HCID 22406609, compound

https://huagongshe.com/reaction/1975691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantBenzyl BromideHCID 7498—
Reactant(3-Methoxyphenyl)acetonitrileHCID 88310—
ProductHCID 22406609HCID 2240660920%

Reaction Steps

The procedures described in the portion of Example 1 which is concerned with the preparation of starting materials were repeated except that 3-methoxyphenylacetonitrile was alkylated in turn with ethyl iodide and benzyl bromide. The 2-benzyl-2-(3-methoxyphenyl)butyronitrile so obtained was treated with boron tribromide to give the required starting material in an overall yield of 20% as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288742
Source datasetuspto-grants-1994_02
ORD IDord-3a56c2cd14124759be26f3f25827ccf7
Source noteuspto-grants-1994_02