A mild and efficient modified Hofmann rearrangement

Journal of Organic Chemistry

Volumn 62, Issue 21, 1997, Pages 7495-7496

  Huang, Xicai ^a   Seid, Mehran ^a   Keillor, Jeffrey W ^a  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BENZAMIDES; CARBOXAMIDES; HOFMANN REARRANGEMENT; PRIMARY AMINES; ROOM TEMPERATURE; TETRABUTYLAMMONIUM TRIBROMIDE; TO EFFECT;

CHEMISTRY;

ORGANIC COMPOUNDS;

EID: 0001329449     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo9708553     Document Type: Article

References (18)

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13. + + 1)) 202.17990
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18. Furthermore, when the reaction of benzamide with NBS in the presence of DBU is carried out in benzyl alcohol, the corresponding benzyl carbamate is isolated in 76% yield. When the reaction is carried out in water, aniline is obtained directly in 50% yield.