돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133812생성일: 2026년 10월 26일

Acetic Acid → Ethyl (2Z)-3,4-dihydro-1(2H)-naphthalenylidene(formylamino)ethanoate

https://huagongshe.com/reaction/133812

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-TetraloneHCID 68266—
반응물Ethyl isocyanoacetateHCID 533707—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물Ethyl (2Z)-3,4-dihydro-1(2H)-naphthalenylidene(formylamino)ethanoateHCID 5973609245%

반응 단계

To a stirred slurry of potassium t-butoxide (4.7 g, 42.0 mmol) in 30 mL tetrahydrofuran at 0° C. is added ethyl isocyanoacetate (4.53 g, 40.0 mmol). This is stirred for 30 mins whereupon a solution of β-tetralone (5.88 g, 40.0 mmol) in tetrahydrofuran (20 mL) is added dropwise. The reaction mixture is allowed to warm to room temperature and stirred for 3 hours. The reaction mixture is then recooled in an ice bath and to this is added acetic acid (2.5 g, 41.6 mmol), allowed to warm to room temperature and stirred for an additional 30 mins. The solvent is removed in-vacuo and the residue partitioned between water and ethyl acetate. The organic layer is washed with water and brine, dried over sodium sulfate, filtered, evaporated and crystallized from cyclohexane to give 4.67 g of a white solid (contains some E-isomer), MS: m/z 260.2 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390910B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-a8160e7125b049a2b8a174406f9a3c0f
출처 메모uspto-grants-2008_06