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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356594Generated: October 30, 2026

p-Tolunitrile → HCID 59384156, compound

https://huagongshe.com/reaction/2356594

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-TolunitrileHCID 7724—
ReactantTetrahydrofuranHCID 8028—
Reactant1,4-Benzodioxan-6-ylamineHCID 89148—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 178425626HCID 178425626—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 59384156HCID 59384156—

Reaction Steps

N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-4-methylbenzenecarboxamidine To a solution of 0.605 g (4.0 mmol) of 1,4-benzodioxan-6-amine in 5 mL of tetrahydrofuran at ambient temperature was added 2.2 ml (4.4 mmol) of 2.0 M (in tetrahydrofuran) sodium bis(trimethylsilyl)amide and the resulting solution was stirred for 20 min. To this reaction mixture was slowly added a solution of 0.47 g (4.0 mmol) of p-tolunitrile in 2 mL of tetrahydrofuran. The resulting mixture was stirred at ambient temperature for 5 hrs and then poured into brine (25 mL) and dichloromethane (50 mL). The organic layer was separated and the aqueous layer was extracted with 25 mL of dichloromethane (25 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to yield the title compound as brown crystalline solid, which was used without further purification. LC/MS 269.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759352B2
Source datasetuspto-grants-2010_07
ORD IDord-398dc48fff01402ba0e428decceee10d
Source noteuspto-grants-2010_07