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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416535Generated: November 2, 2026

Phenacylamine → HCID 21841526, compound

https://huagongshe.com/reaction/1416535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacylamineHCID 11952—
ReactantAmmonium ChlorideHCID 25517—
ReactantEther tetrahydrofuranHCID 21868444—
ReactantHCID 178418816HCID 178418816—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21841526HCID 21841526—

Reaction Conditions

Temperature15 °C

Reaction Steps

After dissolving 44.4 mmol of isobutylmagnesium bromide (2M ether solution) in 30 ml of a solvent mixture: ether/THF=1:1, a solution containing 2.0 g (14.8 mmol) of 2-aminoacetophenone in 10 ml of THF was added dropwise while maintaining the internal temperature at 15° C. or less. After stirring at 15° C. for an hour, the reaction mixture was poured into a saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 2.9 g of the desired product as an yellow oil. Yield was quantitative.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05914344
Source datasetuspto-grants-1999_06
ORD IDord-3752248536144c4daacb1482bb88050d
Source noteuspto-grants-1999_06