돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33447생성일: 2026년 10월 23일

Dimethylformamide dimethyl acetal → ethyl 4-[(2E)-3-(dimethylamino)prop-2-enoyl]benzoate

https://huagongshe.com/ko/reaction/33447

반응식

참여 물질

역할이름HCID투입량
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물Ethyl 4-acetylbenzoateHCID 600911—
생성물ethyl 4-[(2E)-3-(dimethylamino)prop-2-enoyl]benzoateHCID 21906035—

반응 단계

A mixture of ethyl 4-acetylbenzoate (3.00 g, 15.62 mmol) and N,N-dimethylformamide dimethyl acetal (6.2 g, 52.10 mmol) was refluxed for 18 hours, cooled and concentrated to give ethyl 4-[(2E)-3-(dimethylamino)prop-2-enoyl]benzoate quantitatively. A solution of ethyl 4-[(2E)-3-(dimethylamino)prop-2-enoyl]benzoate, potassium carbonate (3.55 g, 25.74 mmol), and 4-(amidinoamino)benzamide (3.10 g, 12.87 mmol) in ETOH (120 mL) was refluxed for 18 hours. The mixture was cooled, filtered, and washed with ETOH, water, then ether respectively to give ethyl 4-{2-[(4-carbamoylphenyl)amino]pyrimidin-4-yl}benzoate (2.60 g, 46% yield). This compound was refluxed for 2 hours in ETOH (30 mL), water (20 mL), and NaOH (0.640 g, 16 mmol). The reaction mixture was cooled, acidified to pH 3, and filtered to give 1.00 gram (42% yield) of the titled compound. HPLC/ES-MS (20-100% acetonitrile): R.T. 4.7 min.(Method A); (m/z) 335 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429599B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-49ccddaa04484f69bc48d6498ae067fa
출처 메모uspto-grants-2008_09