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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1583030생성일: 2026년 10월 27일

4-Methylmorpholine → n,n-Di-n-pentyl-2-methoxy-5-formylbenzamide

https://huagongshe.com/reaction/1583030

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물DipentylamineHCID 16316—
반응물HOAtHCID 181649—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물5-Formyl-2-methoxybenzoic acidHCID 3926683—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물n,n-Di-n-pentyl-2-methoxy-5-formylbenzamideHCID 2271681999.8%

반응 단계

Di-n-pentylamine (873 mg, 5.55 mmol, 2 eq) was added to a solution of 2-methoxy-5-formylbenzoic acid (500 mg, 2.78 mmol, 1 eq), 1-hydroxy-7-azabenzotriazole (755 mg, 5.55 mmol, 2 eq), and N-methylmorpholine (0.83 mL, 7.58 mmol, 2.73 eq) in N,N-dimethylformamide (10 mL). To this was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.06 g, 5.55 mmol, 2 eq) and the reaction mixture stirred overnight. The reaction mixture was diluted with ethyl acetate (20 mL) and washed sequentially with 10% HCl (3×20 mL), brine (20 mL), saturated aqueous sodium bicarbonate (2×20 mL) and brine (20 mL). The organic solution was dried over sodium sulfate and evaporated in vacuo to give the product as a pale brown oil (886 mg, 99%). 1H NMR (CDCl3) δ9.83 (s, 1H, O═C—H), 3.85 (s, 3H, OCH3), 3.52 (m, 1H, NCH2), 3.38 (m, 1H, NCH2), 2.98 (m, 2H, NCH2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06740670B2
출처 데이터셋uspto-grants-2004_05
ORD IDord-49f92be5173f42138ec1ae5aee200f28
출처 메모uspto-grants-2004_05