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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880341Generated: October 30, 2026

Acetic Acid → HCID 66920530, compound

https://huagongshe.com/reaction/1880341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethylglyoxalHCID 880—
ReactantSodium ChlorideHCID 5234—
Reactant(Tetrahydrofuran-3-yl)hydrazine hydrochlorideHCID 19432761—
SolventWaterHCID 962—
ProductHCID 66920530HCID 6692053053%

Reaction Steps

Acetic acid (1.7 mL) was slowly added to a solution of tetrahydrofuran-3-ylhydrazine hydrochloride (2.50 g, 18.0 mmol) (prepared as described by Bacon, E. R.; Singh, B.; and Lesher, G. Y. in U.S. Pat. No. 5,294,612) in water (30 mL). This mixture was then added dropwise to a solution of pyruvaldehyde (2.59 g, 2.34 mL, 14.4 mmol) in water (240 mL). The mixture was stirred overnight at room temperature. The mixture was poured into a seperatory funnel, NaCl was added and dissolved in the aqueous phase and then extracted with CH2Cl2 (6-times). The combined organic extracts were dried over Na2SO4, filtered and concentrated to provide crude material, which was purified by preadsorbing the oil on SiO2 followed by chromatography (Isco, 80 g RediSep column) eluting with a 0-80% EtOAc/heptane gradient over 80 minutes. Analysis of fractions resulted in isolation of 2-oxopropanal tetrahydrofuran-3-ylhydrazone (1.19 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318762B2
Source datasetuspto-grants-2012_11
ORD IDord-c0b42638945343b8864f0e1d528c697f
Source noteuspto-grants-2012_11