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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349369Generated: October 30, 2026

Imidazole → (4-Iodo-but-2-ynyloxy)-acetonitrile

https://huagongshe.com/reaction/349369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-Hydroxy-but-2-ynyloxy)-acetonitrileHCID 86012515—
SolventDichloromethaneHCID 6344—
Product(4-Iodo-but-2-ynyloxy)-acetonitrileHCID 8601251692%

Reaction Steps

Triphenylphosphine (10.94 g, 41.7 mmol) and iodine (10.55 g, 41.6 mmol were added sequentially to a solution of (4-hydroxy-but-2-ynyloxy)-acetonitrile (4.35 g, 34.8 mmol) in CH2Cl2 (100 mL). The reaction mixture became homogeneous after 5 min at rt and imidazole (2.76 g, 40.5 mmol) was added slowly in small portions. After 1.5 h at rt, the reaction was filtered through activity I basic alumina, washing with 20% EtOAc/Hexane. The filtrate was concentrated in vacuo then purified by flash column chromatography on silica gel (hexane→10% EtOAc/hexane, gradient) to afford 7.51 g (92%) of (4-iodo-but-2-ynyloxy)-acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179820B2
Source datasetuspto-grants-2007_02
ORD IDord-9b79928d940f40fb95dddc7f4bb9f9ef
Source noteuspto-grants-2007_02