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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2112040생성일: 2026년 10월 27일

2-Methoxyphenylacetic acid → N-heptyl-2-(2-methoxyphenyl)acetamide

https://huagongshe.com/reaction/2112040

반응식

참여 물질

역할이름HCID투입량
반응물2-Methoxyphenylacetic acidHCID 7134—
반응물1-HeptanamineHCID 8127—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-heptyl-2-(2-methoxyphenyl)acetamideHCID 337599587.5%

반응 조건

온도0 °C

반응 단계

Heptan-1-amine (1 g, 8.679 mmol was dissolved in DMF (10 ml), (2-methoxyphenyl)acetic acid (1.587 g, 9.547 mmol) was added and the mixture was cooled to 0° C. N-[(1H-1,2,3-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methylmethanaminium tetrafluoroborate (3.065, 9.547 mmol) and N-ethyl-N,N-diisopropylamine (2.356 g, 18.226 mmol) were added. The solution was stirred overnight at room temperature. EtOAc (20 ml) was added and the organic phase was washed with two portions of NaHCO3 (2×20 ml, aq). The organic layer was dried (MgSO4) and the solvent was removed by evaporation. The crude was purified by preparative HPLC (started with isocratic acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min). The product containing fractions were pooled and the acetonitrile was removed by evaporation EtOAc (10 ml) was added and the organic phase was washed with two portions of brine and dried (MgSO4) and the solvent was removed by evaporation to give 2.00 g of N-heptyl-2-(2-methoxyphenyl)acetamide (yield 87.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07521461B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-ac1fe9d7f8f843638cb2d91c81943f64
출처 메모uspto-grants-2009_04