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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63617Generated: October 26, 2026

Trimethylsilyl cyanide → HCID 82623563, compound

https://huagongshe.com/reaction/63617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant7-bromo-3,4-dihydro-2H-1-benzopyran-4-oneHCID 22335736—
Catalystzinc(II)iodideHCID 9883512—
SolventTolueneHCID 1140—
ProductHCID 82623563HCID 8262356379.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 7-bromochroman-4-one (5.00 g, 22.0 mmol) and ZnI2 (30 mg) in toluene (50 mL) was added TMSCN (4.36 g, 44.0 mmol), and the mixture was heated at 60° C. overnight. The reaction mixture was cooled to rt, and a solution of LAH (20.0 mL, 2.4 M in THF, 44.0 mmol) was added slowly. The mixture was stirred at 40° C. for 2 h. The reaction was quenched with the addition of EtOAc (10 mL) at 0° C., followed by water (5 mL) and aqueous 10% NaOH (5 mL). The reaction mixture was diluted with EtOAc, dried (MgSO4), filtered through Celite, and concentrated to give 4.5 g (79%) of the crude 4-(aminomethyl)-7-bromo-3,4-dihydro-2H-1-benzopyran-4-ol intermediate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447046B2
Source datasetuspto-grants-2016_09
ORD IDord-0ac686a3c07b4d78994868ae452911bf
Source noteuspto-grants-2016_09