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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042535Generated: November 2, 2026

Thiophene-3-carboxylic acid → HCID 12796524, compound

https://huagongshe.com/reaction/2042535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophene-3-carboxylic acidHCID 6918—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantPotassium PermanganateHCID 516875—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12796524HCID 12796524—

Reaction Steps

A solution of 3-thiophenecarboxylic acid (10 g, 78 mmol) in 250 mL of THF at 0° C. under N2 was added 2.0 M LDA (2.2 eq., 86 mL) dropwise. After 10 min at 0° C., p-anisaldehyde (10.6 mL, 1.12 eq.) was added and the mixture was slowly warmed to room temperature overnight. The reaction was stirred for ˜14 h, after which 100 mL of ice-water was added, and the solvent was evaporated. The aqueous solution was washed with EtOAc (2×40 mL), and then added KMnO4 (2 eq., 12.4 g) dropwise at 0° C. The ice-bath was removed and the reaction was heated to 60° C. for 3 h. The solid was collected and washed with hot water. The aqueous layer was acidified to pH ˜3, extracted with EtOAc (3×50 mL). The combined EtOAc was dried and evaporated. The crude solid was dissolved in 50 mL of EtOH, and NH2NH2.H2O (1.5 eq., 1.5 mL) was added dropwise. The reaction was heated to 80° C. for 3 h, and the resulting solid was collected and washed with EtOH to give 3.6 g (36%): MS m/z 259 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586588B2
Source datasetuspto-grants-2013_11
ORD IDord-52671026debe4b20bf37cc60cced5dd1
Source noteuspto-grants-2013_11