تفاعل #2437
ord-b0e3813329fd4701a3a3f986ee306d00
معادلة التفاعل
NaN3
Et3N
ethyl chloroformate
3-(N-tert-butoxylcarbonyl-N-methylamino)benzoic acid
→
title compound
المردود 78.5%
3-(N-tert-Butoxylcarbonyl-N-methylamino)phenyl isocyanate
المردود 78.5%
الكواشف
لا شيء
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1workup.STIRRINGThe mixture was stirred at the same temperature for a further 1 h
- 2غسيلThe organic portion was washed with brine
- 3درجة الحرارةrefluxed for 2 h
- 4أخرىevaporated
- 5workup.DISTILLATIONThe residue was distilled (100°-105° C./0.9-1.0 mmHg)
الإجراء التجريبي
Et3N (3.71 g, 36.7 mmol) and a solution of ethyl chloroformate (4.31 g, 39.7 mmol) in acetone (10 ml) were successively added dropwise to a solution of 3-(N-tert-butoxylcarbonyl-N-methylamino)benzoic acid (8.0 g, 31.8 mmol) in acetone (64 ml) below 5° C. After stirring for 30 min, a solution of NaN3 (3.10 g, 47.7 mmol) in water (10 ml) was added to the solution below 5° C. The mixture was stirred at the same temperature for a further 1 h, then poured into toluene (80 ml) and water (160 ml). The organic portion was washed with brine, refluxed for 2 h and evaporated. The residue was distilled (100°-105° C./0.9-1.0 mmHg) to afford the title compound (6.2 g, 78%) as a yellow oil.