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HRID 232008Erstellt: 24. Oktober 2026

Triethylamine → Phenyl 1H-benzo[d][1,2,3]triazol-5-ylcarbamate

https://huagongshe.com/de/reaction/232008

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPhenyl chloroformateHCID 15891—
EduktDimethylacetamideHCID 31374—
EduktHCID 178478652HCID 178478652—
LösungsmittelWaterHCID 962—
LösungsmittelPyridineHCID 1049—
ProduktPhenyl 1H-benzo[d][1,2,3]triazol-5-ylcarbamateHCID 17852183588,5%

Reaktionsschritte

500 ml of dimethylacetamide was added to 62.1 g of 5-aminobenzotriazole dihydrochloride, and 83.7 ml of triethylamine was dropwise added thereto with cooling in an ice bath. Further, 21.0 ml of pyridine was dropwise added, followed by dropwise addition of 42.3 g of phenyl chlorocarbonate at 5° C. or lower, and then, the whole was stirred for 2 hours at room temperature. After the reaction, the reaction solution was poured into 2 liters of water for crystallization, and the crystal formed was taken out by filtration to obtain 60.8 g of 5-phenoxycarbonylaminobenzotriazole. To 5.1 g of 5-phenoxycarbonylaminobenzotriazole thus-obtained was added 40 ml of acetonitrile, and 2.6 g of N,N-diethylethylenediamine was dropwise added thereto with stirring at 45° C., and then the whole was stirred for 2 hours as such. After the reaction, the reaction solution was cooled in an ice bath, and the crystal precipitate was taken out by filtration and recrystallized from 60 ml of a mixed solvent of methyl alcohol/acetonitrile (1/5) to obtain 3.8 g of the desired product. M.P.: 149°-150° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04851321
Quelldatensatzuspto-grants-1989_07
ORD IDord-d72ff68322884e16b72edaf0be0e42fa
Quellennotizuspto-grants-1989_07