pentadecan-8-amine

Conditions: temp:135.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Under protective gas, a mixture of 3 g (7.48 mmol) of 9-bromoperylene-3,4-dicarboxylic anhydride and 8 g (35 mmol) of 1-heptyloctylamine in 150 ml of N-methylpyrrolidone and 3 ml of acetic acid was heated to 135° C. for 20 h.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 5 g (18 mmol) of 4-bromonaphthalene-1,8-dicarboxylic anhydride were heated to 160° C. with 6.1 g (27 mmol) of 1-heptyloctylamine in 50 ml of ethylene glycol for 4 hours. The resulting solution was allowed to cool to room temperature. Thereafter, the solution was diluted with 50 ml of methanol and 50 ml of distilled water. The aqueous solution was extracted with diethyl ether, the solution was dried over MgSO4 and the solvent was evaporated. The resulting yellow oil was purified by column chromatography with dichloromethane as the eluent, which afforded 5.5 g (63%) of the title compound as a colorless oil. The aqueous solution was extracted with diethyl ether the solution was dried over MgSO4 the solvent was evaporated The resulting yellow oil was purified by column chromatography with dichloromethane as the eluent, which

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 5 g (18 mmol) of 4-bromonaphthalene-1,8-dicarboxylic anhydride were heated to 160° C. with 6.1 g (27 mmol) of 1-heptyloctylamine in 50 ml of ethylene glycol for 4 hours. The resulting solution was allowed to cool to room temperature. Thereafter, the solution was diluted with 50 ml of methanol and 50 ml of distilled water. The aqueous solution was extracted with diethyl ether, the solution was dried over MgSO4 and the solvent was evaporated. The resulting yellow oil was purified by column chromatography with dichloromethane as the eluent, which afforded 5.5 g (63%) of the title compound as a colorless oil. The aqueous solution was extracted with diethyl ether the solution was dried over MgSO4 the solvent was evaporated The resulting yellow oil was purified by column chromatography with dichloromethane as the eluent, which

Conditions: temp:135.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Under protective gas, a mixture of 3 g (7.48 mmol) of 9-bromoperylene-3,4-dicarboxylic anhydride and 8 g (35 mmol) of 1-heptyloctylamine in 150 ml of N-methylpyrrolidone and 3 ml of acetic acid was heated to 135° C. for 20 h.

Conditions: temp:135.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Under protective gas, a mixture of 3 g (7.48 mmol) of 9-bromoperylene-3,4-dicarboxylic anhydride and 8 g (35 mmol) of 1-heptyloctylamine in 150 ml of N-methylpyrrolidone and 3 ml of acetic acid was heated to 135° C. for 20 h.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 5 g (18 mmol) of 4-bromonaphthalene-1,8-dicarboxylic anhydride were heated to 160° C. with 6.1 g (27 mmol) of 1-heptyloctylamine in 50 ml of ethylene glycol for 4 hours. The resulting solution was allowed to cool to room temperature. Thereafter, the solution was diluted with 50 ml of methanol and 50 ml of distilled water. The aqueous solution was extracted with diethyl ether, the solution was dried over MgSO4 and the solvent was evaporated. The resulting yellow oil was purified by column chromatography with dichloromethane as the eluent, which afforded 5.5 g (63%) of the title compound as a colorless oil. The aqueous solution was extracted with diethyl ether the solution was dried over MgSO4 the solvent was evaporated The resulting yellow oil was purified by column chromatography with dichloromethane as the eluent, which

Conditions: temp:135.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Under protective gas, a mixture of 3 g (7.48 mmol) of 9-bromoperylene-3,4-dicarboxylic anhydride and 8 g (35 mmol) of 1-heptyloctylamine in 150 ml of N-methylpyrrolidone and 3 ml of acetic acid was heated to 135° C. for 20 h.