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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456791Generated: October 26, 2026

Hydrochloric Acid → 4,4-Diethoxy-1-(4-nitrophenyl)but-2-yn-1-one

https://huagongshe.com/reaction/456791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,3-DiethoxypropyneHCID 66285—
ReactantN-methoxy-N-methyl-4-nitrobenzamideHCID 2991007—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4,4-Diethoxy-1-(4-nitrophenyl)but-2-yn-1-oneHCID 18438594—

Reaction Conditions

Temperature-70 °C

Reaction Steps

3,3-Diethoxyprop-1-yne (8.5 ml, 59 mmol) was dissolved in THF (100 ml). The solution was cooled to −70° C., and nBuLi (19 ml of 2.5 M soln in hexanes, 47.5 mmol) was added over 5 min. The solution was warmed to 0° C. for 15 min, then cooled to −70 ° C. again. A solution of N-methoxy-N-methyl-4-nitrobenzamide (Intermediate 8, 8.04 g, 38.1 mmol) in THF (50 ml) was added dropwise over 15 min. The solution was warmed to 0° C. after 15 min, and held there for 45 min. The reaction mixture was poured into 1M HCl, extracted with ethyl acetate and dried over sodium sulfate. Purification by chromatography on silica gel eluting with 30 to 50% dichloromethane: hexane, gave the title compound as a light orange oil which solidified on standing (7.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186738B2
Source datasetuspto-grants-2007_03
ORD IDord-52ad3e59f4f24aa3a7736f9b578531f6
Source noteuspto-grants-2007_03