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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650931Generated: October 26, 2026

Trimethyl orthovalerate → 2-(1-n-Butyl-1-methoxymethyleneamino)-thiophene-3-carboxylicacid propylamide

https://huagongshe.com/reaction/650931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthovalerateHCID 83755—
Reactant2-amino-N-propylthiophene-3-carboxamideHCID 11788675—
SolventMethanolHCID 887—
Product2-(1-n-Butyl-1-methoxymethyleneamino)-thiophene-3-carboxylicacid propylamideHCID 53928955—

Reaction Conditions

Temperature130 °C

Reaction Steps

In a destillation apparatus, a mixture of 1.84 g of 2-aminothiophene-3-carboxylic-acid propylamide and 2.43 g of trimethyl orthovalerate is heated for 2 hours at 130° C. Methanol, which arises during the reaction is directly distilled out of the reaction flask. After cooling, the crude product is purified by column chromatography (eluant:hexane/ethylacetate=1:2). Yield:1.9 g pure 2-(1-n-butyl-1-methoxymethyleneamino)thiophene-3-carboxylic-acid propylamide; m.p. 68-70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277858B1
Source datasetuspto-grants-2001_08
ORD IDord-8a79abdb323e46cabeab776212a780a5
Source noteuspto-grants-2001_08