Intramolecular cyclization of N-acetyl-6-(cyclopent-1-enyl)-2-methylaniline

DOI: 10.1007/BF02494577

Source and publish data:

Russian Chemical Bulletin p. 396 - 397 (1999)

Update date:2022-08-18

Topics:

Authors:

Gataullin, R. R.

Afon'kin, I. S.

Pavlova, I. V.

Abdrakhmanov, I. B.

Tolstikov, G. A.

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Article abstract of DOI:10.1007/BF02494577

N-Acetyl-6-(cyclopent-1-enyl)-2-methylaniline underwent intramolecular cyclization in the presence of HCl in CH2Cl2 at 20 deg C to form 2,8-dimethylspiro[cyclopentane-1,4'-4'H-3,1-benzooxazine] in quantitative yield.

Full text of DOI:10.1007/BF02494577

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