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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294951Generated: November 2, 2026

Hydrochloric Acid → 1-Phenyl-3-buten-2-one

https://huagongshe.com/reaction/2294951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-Methoxy-N-methyl-2-phenylacetamideHCID 10419762—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product1-Phenyl-3-buten-2-oneHCID 3773473%

Reaction Steps

A 1M solution of vinylmagnesium bromide in THF (80 mL, 80 mmol) was added dropwise to a stirred solution of N-methoxy-N-methylphenylacetamide (12.8 g, 71.5 mmol) in distilled tetrahydrofuran (THF) (200 mL), cooled to 0°-5° C. in an ice-water bath. The solution was stirred at 0°-5° C. for 2 h and was then poured into cold 1N HCl solution (150 mL). The THF layer was separated and the aqueous (aq.) layer was extracted with EtOAc (100 mL). Organic extracts were combined, dried (MgSO4), filtered and concentrated. The crude oil was chromatographed on a silica gel column and eluted with 5-20% ethylacetate (EtOAc) in hexanes to obtain title 4-phenyl-but-1-ene-3-one (7.62 g, 73%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691356
Source datasetuspto-grants-1997_11
ORD IDord-fe12891b8b7a4109899edadd3de55e0a
Source noteuspto-grants-1997_11