RI 7529 Thermal Reactions Of 1-Methylindole

The National Institute for Occupational Safety and Health (NIOSH)
Irven A. Jacobson
Organization:
The National Institute for Occupational Safety and Health (NIOSH)
Pages:
11
File Size:
457 KB
Publication Date:
Jan 1, 1971

Abstract

The thermal reactions of l-methylindole were studied in the temperature range of 525° to 627° C in a flow reactor. The major products consisted of 2-methylindole, 3-methylindole, indole, quinoline, hydrogen, and methane. 2-Methylindole is formed from 1-methylindole by an irreversible isomerization reaction. The 2-methylindole isomerizes in a reversible manner to 3-methyl-indole, the equilibrium favoring the 3-methyl isomer. Indole is formed directly from 1-methylindole. Quinoline is formed from l-methylindole, 2-methylindole, and 3-methylindole.
Citation

APA: Irven A. Jacobson  (1971)  RI 7529 Thermal Reactions Of 1-Methylindole

MLA: Irven A. Jacobson RI 7529 Thermal Reactions Of 1-Methylindole. The National Institute for Occupational Safety and Health (NIOSH), 1971.

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