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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293320Generated: October 31, 2026

Acetic Acid → HCID 18937643, compound

https://huagongshe.com/reaction/2293320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl propiolateHCID 12182—
ReactantHCID 18937665HCID 18937665—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18937643HCID 18937643105.2%

Reaction Steps

1.5N butyllithium (19.3 ml, 29.0 mmole) was added under the argon atmosphere to a solution of diisopropylamine (4.3 ml, 30.6 mmole) in tetrahydrofuran (50 ml) at -78° C., and the mixture was stirred for 1 hour. Next, ethyl propiolate (2.4 ml, 23.7 mmole) and a solution of 4-methoxymethoxy-2-nitrobenzaldehyde (3.6 g, 17.0 mmole) in tetrahydrofuran (35 ml) were added in this sequence, and the reaction mixture was stirred at -78° C. for further 2 hours. After a solution of acetic acid (5.0 ml, 87.5 mmole) in tetrahydrofuran (20 ml) and water were sequentially added, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with dilute hydrochloric acid, water, 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(4-methoxymethoxy-2-nitrophenyl)-2-butynoate as an oil (5.53 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686442
Source datasetuspto-grants-1997_11
ORD IDord-e6ac757c8f5947a1921d7e2e218cd0b2
Source noteuspto-grants-1997_11