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HRID 2396867作成日:2026年10月26日

Methanol → 4,4'-Bis(4-aminobenzamido)-3,3'-dihydroxybiphenyl

https://huagongshe.com/reaction/2396867

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物TriethylamineHCID 8471—
反応物4-Nitrobenzoyl chlorideHCID 8502—
反応物3,3'-DihydroxybenzidineHCID 16918—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物4,4'-Bis(4-aminobenzamido)-3,3'-dihydroxybiphenylHCID 1898644799.7%

反応条件

温度0 °C

反応手順

35.0 g (0.162 moles) of 3,3'-dihydroxy-4,4'-diaminobiphenyl and 36.0 g (0.356 moles) of triethylamine were dissolved in a mixed solvent of 300 ml of tetrahydrofuran and 300 ml of N,N-dimethylformamide (DMF) and cooled down to 0° C. Thereafter, a solution of 63.1 g (0.340 moles) of p-nitrobenzoyl chloride in 150 ml of tetrahydrofuran was dropped in the solution in such a way that the resultant reaction solution had a temperature not higher than 10° C. Subsequently, the reaction solution was poured into one liter of methanol thereby permitting the resulting reaction product to be precipitated, followed by filtering, washing with tetrahydrofuran, then with water and finally with methanol, and drying to obtain crude red crystals of 4,4'-bis(4-aminobenzamido)-3,3'-dihydroxybiphenyl. The yield was 82.1 g (at a yield of 99.7%). The crude crystals were recrystallized from a mixed solvent of dimethylformamide and methanol to obtain a pure product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05494991
出典データセットuspto-grants-1996_02
ORD IDord-360cd188f6e5401f8bc5216d044f15d7
出典メモuspto-grants-1996_02