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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448710Generated: October 26, 2026

Cyclohexanecarboxylic acid → N-(5-Phenylthiophen-2-yl)cyclohexanecarboxamide

https://huagongshe.com/reaction/1448710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxylic acidHCID 7413—
ReactantN-(3-carboxy-methyl-5-phenyl-2-thienyl)-cyclohexane carboxamideHCID 70592634—
ReactantHCID 178526965HCID 178526965—
Solvent2,4,6-TrimethylpyridineHCID 7953—
ProductN-(5-Phenylthiophen-2-yl)cyclohexanecarboxamideHCID 23341601—

Reaction Steps

This compound (m.p. 174° C.) was prepared from N-(3-carboxy-methyl-5-phenyl-2-thienyl)-cyclohexane carboxamide (31.1 g, 0.1 mole) and LiI.2H2O (48.1 g, 0.32 mole) by refluxing in collidine (125 ml.) according to the procedure of Example 53 (a). This compound was also prepared according to the procedure of Example 53(b), using cyclohexane carboxylic acid as the acylating agent. The products of the two processes were spectrally identical and had a melting point of 175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04187232
Source datasetuspto-grants-1980_02
ORD IDord-7bedc89a3e994f288dc872cc93d3c31b
Source noteuspto-grants-1980_02