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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293322Generated: October 30, 2026

Acetic Acid → HCID 18937576, compound

https://huagongshe.com/reaction/2293322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl propiolateHCID 12182—
ReactantHCID 11550252HCID 11550252—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18937576HCID 18937576135.8%

Reaction Steps

1.5N butyllithium (14.9 ml, 22.4 mmole) was added under the argon atmosphere to a solution of diisopropylamine (3.3 ml, 23.8 mmole) in tetrahydrofuran (40 ml) at -78° C., and the mixture was stirred for 1.5 hours. Next, a solution of ethyl propiolate (2.7 ml, 26.8 mmole) in tetrahydrofuran (10 ml) and a solution of 5-methoxymethoxy-2-nitrobenzaldehyde (3.15 g, 14.9 mmole) in tetrahydrofuran (10 ml) were added in this sequence, and the reaction mixture was stirred at -78° C. for further 1 hour. After a solution of acetic acid (2.6 ml, 46.2 mmole) in tetrahydrofuran (10 ml) was added, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with dilute hydrochloric acid, a saturated aqueous sodium hydrogen carbonate solution and a saturated aqueous saline in this sequence. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was removed under reduced pressure to give ethyl 4-hydroxy-4(5-methoxymethoxy-2-nitrophenyl)-2-butynoate as an oil (6.26 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686442
Source datasetuspto-grants-1997_11
ORD IDord-4a5c70da3798415ab8bdd6a37d0bc060
Source noteuspto-grants-1997_11