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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399751Generated: October 30, 2026

Potassium Iodide → HCID 54415333, compound

https://huagongshe.com/reaction/2399751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium hydrideHCID 24758—
Reactant4-(Benzoxazol-2-yl)benzyl bromideHCID 11033515—
ReactantHCID 19384402HCID 19384402—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54415333HCID 54415333—

Reaction Steps

To a mixture of 2-triphenylmethylaminomethyl-1-hydroxymethylcyclopropane (0.338 g; 0.984 mmol) in 30 ml THF and 5 ml DMF is added sodium hydride (60%; 0.059 g; 1.48 mmol) followed by 4-(benzoxazol-2-yl)benzyl bromide (0.255 g; 0.886 mmol) and a pinch of potassium iodide. This is stirred overnight, quenched with water, concentrated in vacuo and flash chromatographed using hexane:ethyl-acetate; 7:1 to obtain trans-2-triphenylmethylaminomethyl-[4-(benzoxazol-2-yl)-benzyloxymethyl]cyclopropane as a pale yellow oil which is used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451596
Source datasetuspto-grants-1995_09
ORD IDord-bbf3f3809e4e43489c64016ad1fdf932
Source noteuspto-grants-1995_09