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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781492Generated: October 30, 2026

Bromoacetonitrile → HCID 19045725, compound

https://huagongshe.com/reaction/1781492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantDiphenylacetaldehydeHCID 13696—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19045725HCID 19045725—

Reaction Steps

To a solution of diphenylacetoaldehyde (1 g) in tetrahydrofuran (10 ml) was added a suspension of 60% sodium hydride (0.25 g) in tetrahydrofuran (5 ml) carefully dropwise under ice-cooling and stirring. After completion of dropwise addition, the mixture was further stirred for 20 minutes. Then, bromoacetonitrile (0.41 ml) was added and the mixture was further stirred for 30 minutes. The reaction mixture was poured in ice-water and the oil that had separated out was extracted into ethyl acetate. The organic layer was taken, washed with water, dried over anhydrous sodium sulfate, and concentrated to dryness. The group was purified by silica gel column chromatography to provide the title compound (0.85 g) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633248
Source datasetuspto-grants-1997_05
ORD IDord-0a967e5e88454d92891b438873ad9c10
Source noteuspto-grants-1997_05