Pentethylcyclanone

Pentethylcyclanone
	File:Pentethylcyclanone.png
Clinical data
Other names	Ciclexanona, cyclexanonum, cyclexanone
Identifiers
	IUPAC name 2-(Cyclopenten-1-yl)-2-(2-morpholin-4-ylethyl)cyclopentan-1-one;
CAS Number	15301-52-7 check;
PubChem CID	10355398;
ChemSpider	8530850 check;
UNII	2OU4KS37EO;
E number	{{#property:P628}}
CompTox Dashboard (EPA)	{{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).;
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C16H25NO2
Molar mass	263.381 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C1CC=C(C1)C2(CCCC2=O)CCN3CCOCC3;
	InChI InChI=1S/C16H25NO2/c18-15-6-3-7-16(15,14-4-1-2-5-14)8-9-17-10-12-19-13-11-17/h4H,1-3,5-13H2 check; Key:KUOYUNPLUMKQIF-UHFFFAOYSA-N check;

Pentethylcyclanone is an antitussive medication.^[1]

Synthesis

Pentethylcyclanone can be prepared by alkylation of the anion of the self-condensation product of cyclopentanone with N-(2-chloroethyl)-morpholine.^[2]^[1]

File:Cyclexanone synthesis.png

Cyclexanone synthesis

References

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^ DE 1059901, Ueberwasser H, "Verfahren zur Herstellung von substituierten 2-Amino-alkylcycloalkanonen bzw, ihren Salzen [Process for the preparation of substituted 2-amino-alkylcycloalkanones or their salts]", published Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value)., assigned to Ciba AG

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[2] DE 1059901, Ueberwasser H, "Verfahren zur Herstellung von substituierten 2-Amino-alkylcycloalkanonen bzw, ihren Salzen [Process for the preparation of substituted 2-amino-alkylcycloalkanones or their salts]", published Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value)., assigned to Ciba AG

[1]

[2]

Pentethylcyclanone

Synthesis

References

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