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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329565Generated: October 30, 2026

2-Thiophenecarboxaldehyde → HCID 70373074, compound

https://huagongshe.com/reaction/329565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantHCID 13557219HCID 13557219—
SolventEthanolHCID 702—
ProductHCID 70373074HCID 7037307483.2%

Reaction Steps

This compound was prepared in a manner analogous to that of Example 5, using 1.28 grams (0.005 mole) of 2-[(4-amino-2-chlorophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone and 0.56 gram (0.005 mole) of thiophene-2-carboxaldehyde in 25 mL of ethanol. The reaction mixture was concentrated under reduced pressure to a residual oil. The oil was dissolved in anhydrous diethyl ether and was dried for two hours with magnesium sulfate. The mixture was filtered, and the filtrate was concentrated under reduced pressure to yield 1.46 grams of 2-[[2-chloro-4-[(thien-2-yl)methylimino]phenyl]-methyl]-4,4-dimethyl-3-isoxazolidinone as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892578
Source datasetuspto-grants-1990_01
ORD IDord-47ca0499e3a04f0ea951c86fe5fe2125
Source noteuspto-grants-1990_01