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HRID 1017808作成日:2026年10月26日

Triethylamine → Benzanilide

https://huagongshe.com/reaction/1017808

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物Benzyl p-aminobenzoateHCID 98488—
反応物1,4-Benzenedicarboxylic acid, methyl esterHCID 3614454—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物BenzanilideHCID 7168134.8%

反応手順

A solution of mono-methyl terephthalate (4.00 g, 22 mmol) in ethyl acetate (25 mL) and DMF (0.1 mL) was cooled in an ice bath and treated with oxalyl chloride (11 mL, 2N in CH2Cl2, 22 mmol) over 30 minutes. After stirring 2 hours at room temperature the solvent was removed on a rotary evaporator and the residue dissolved in CH2Cl2 (20 mL) and added to a solution of benzyl 4-aminobenzoate (5.00 g, 22 mmol) in CH2Cl2 (25 mL) and triethylamine (4.3 mL, 31 mmol) at −60° C. The reaction mixture was warmed to room temperature for 1 hour and then partitioned between water and ethyl acetate. The ethyl acetate layer was dried over sodium sulfate, filtered, and evaporated. The residue was recrystallized from t-butyl methyl ether to give 5.85 g of compound 8.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479548B2
出典データセットuspto-grants-2002_11
ORD IDord-9f8d21a2aa104ff597679c335e1f7e44
出典メモuspto-grants-2002_11