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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270640Generated: October 31, 2026

Sulfuric Acid → HCID 24259182, compound

https://huagongshe.com/reaction/1270640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantCyanideHCID 5975—
ReactantSodium CyanideHCID 8929—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22640885HCID 22640885—
SolventAcetic AcidHCID 176—
ProductHCID 24259182HCID 2425918241.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Powdered sodium cyanide (1.18 g, 24 mmol) was placed in a flask and covered with 5.5 mL of acetic acid. A mixture of sulfuric acid (3 mL) and acetic acid (2.75 mL) was cooled to 0° C. and then added to the cyanide suspension over a period of 3 minutes. The mixture was stirred for 30 minutes at room temperature, followed by the addition of 1,1-diethyl-2-(4-methoxyphenyl)ethanol (4.6 g, 22 mmol). The mixture was stirred overnight then poured into ice and sodium hydroxide. The product was extracted with ether, and the ether layer dried over anhydrous sodium sulfate, and concentrated. The residue was suspended in 20% sodium hydroxide and refluxed overnight under nitrogen. The reaction was cooled, diluted with water, and extracted with ether. The ether layer was separated, washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by reversed-phase HPLC (C-18 using 0.1% HCl acetonitrile as the elutant) to give 1.91 g of 1,1-diethyl-2-(4-methoxyphenyl)ethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202261B2
Source datasetuspto-grants-2007_04
ORD IDord-a4c42e2ed7974f3e93fe3b2f9a23ebdb
Source noteuspto-grants-2007_04