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HRID 232008作成日:2026年10月25日

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

https://huagongshe.com/reaction/232008

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Phenyl chloroformateHCID 15891—
反応物DimethylacetamideHCID 31374—
反応物HCID 178478652HCID 178478652—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物Phenyl 1H-benzo[d][1,2,3]triazol-5-ylcarbamateHCID 17852183588.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04851321
出典データセットuspto-grants-1989_07
ORD IDord-d72ff68322884e16b72edaf0be0e42fa
出典メモuspto-grants-1989_07