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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731Generated: October 23, 2026

Hydrochloric Acid → 4-(Thiophen-3-yl)butanoic acid

https://huagongshe.com/en/reaction/1731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant[2-Oxo-2-(3-thienyl)ethyl]malonic acidHCID 6611424—
SolventEthylene GlycolHCID 174—
Product4-(Thiophen-3-yl)butanoic acidHCID 1104114387.6%

Reaction Steps

Hydrazine hydrate (1.3 mL, 1.34 g, 26.8 mmol) was added dropwise to a solution of KOH (3.54 g, 63 mmol) and 2-[2-oxo-2-(3-thienyl) ethyl]malonic acid 8(c) (4.00 g, 17.5 mmol) in ethylene glycol (30 mL). This solution was heated at reflux for 6 hours. After cooling to room temperature, the crude reaction mixture was poured into a mixture of 6N HCl (50 mL) and ice (200 g). This aqueous mixture was saturated with NaCl, then extracted with ether (3×70 mL). The combined organic extracts were dried over Na2SO4 and concentrated, in vacuo, to provide an orange oil (2.61 g) of sufficient purity to be employed in the subsequent reaction without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726312
Source datasetuspto-grants-1998_03
ORD IDord-d7d51544825c4bb7a548bd1885f197b6
Source noteuspto-grants-1998_03