돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1099482생성일: 2026년 10월 25일

4-Methylmorpholine → 2-Cyanoethyl 1-isocyanatomethyl-1-Cyclohexane Acetate

https://huagongshe.com/reaction/1099482

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Ethyl chloroformateHCID 10928—
반응물Sodium AzideHCID 33557—
반응물1-[(2-Cyanoethoxycarbonyl)methyl]-1-Cyclohexane Acetic AcidHCID 22340960—
용매TetrahydrofuranHCID 8028—
생성물2-Cyanoethyl 1-isocyanatomethyl-1-Cyclohexane AcetateHCID 8586375264.1%

반응 조건

온도-20 °C

반응 단계

1.5 mL of N-methyl morpholine (13.62 mmol) and 1.3 mL of ethyl chloroformate (13.03 mmol) was added to a solution of 1-[(2-cyanoethoxycarbonyl)-methyl]-1-cyclohexane acetic acid (5) (11.84 mmol) in 30 mL of anhydrous THF at −20° C. under nitrogen atmosphere. The reaction mixture was stirred at −20° C. for 20 minutes, warmed to −5° C., an aqueous solution of NaN3 (29.61 mmol, in 3.5 mL of H2O) was added and then stirred for 30 minutes at −5° C. to −10° C. Then, THF was removed under reduced pressure and the residue was extracted with CH2Cl2 and dried over Na2SO4. After concentration in vacuo the crude product was dissolved in 20 mL of anhydrous toluene and refluxed for 20 minutes. The mixture was cooled to room temperature and toluene was removed under reduced pressure. The residue was purified on silica gel (15% ethyl acetate in hexane) to afford 1.9 g (64%) of the title compound. 1H NMR (CDCl3): δ 4.29 (2H, t, J=6.0 Hz); 3.42 (2H, s); 2.73 (2H, t, J=6.0 Hz); 2.44 (2H, s); 1.49-1.39 (10H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143437B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-1f7de21d5c5f4dc8af6556074fedc954
출처 메모uspto-grants-2012_03