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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1017808생성일: 2026년 10월 26일

Triethylamine → Benzanilide

https://huagongshe.com/reaction/1017808

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물Benzyl p-aminobenzoateHCID 98488—
반응물1,4-Benzenedicarboxylic acid, methyl esterHCID 3614454—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물BenzanilideHCID 7168134.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06479548B2
출처 데이터셋uspto-grants-2002_11
ORD IDord-9f8d21a2aa104ff597679c335e1f7e44
출처 메모uspto-grants-2002_11