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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794679Generated: November 1, 2026

Acetic Acid → Ethyl 4-hydroxy-4-(4,5-dimethoxy-2-nitrophenyl)-2-butynoate

https://huagongshe.com/reaction/1794679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl propiolateHCID 12182—
Reactant6-NitroveratraldehydeHCID 88505—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-hydroxy-4-(4,5-dimethoxy-2-nitrophenyl)-2-butynoateHCID 15672998117.2%

Reaction Steps

1.5 N butyl lithium (26.8 ml, 40.2 mmol) was added to a solution of diisopropylamine (6.0 ml, 42.8 mmol) in tetrahydrofuran (75 ml) under an argon atmosphere at −78° C. The mixture was stirred for one hr. Ethyl propiolate (3.4 ml, 33.5 mmol) and a solution of 4,5-dimethoxy-2-nitrobenzaldehyde (5.0 g, 23.7 mmol) in tetrahydrofuran (50 ml) were added thereto in that order, and the mixture was stirred at −78° C. for additional 1.5 hr. A solution of acetic acid (7.0 ml, 122 mmol) in tetrahydrofuran (20 ml) was added thereto, followed by addition of water. The mixture was extracted with ethyl acetate. The organic layer was washed with dilute hydrochloric acid, water, a saturated aqueous sodium hydrogencarbonate solution, and saturated brine solution in that order. The organic layer was then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give ethyl 4-hydroxy-4-(4,5-dimethoxy-2-nitrophenyl)-2-butynoate as an oil (8.59 g) The resultant ethyl 4-hydroxy-4-(4,5-dimethoxy-2-nitrophenyl)-2-butynoate was dissolved in toluene (80 ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022860B2
Source datasetuspto-grants-2006_04
ORD IDord-8911d84290bc446abcca8bfbdd9ea3e6
Source noteuspto-grants-2006_04