Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetonitrile → Ethyl cyanomethyl(1-(2-nitrophenyl)ethyl)carbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 2-(1-(2-Nitrophenyl)ethylamino)acetonitrile | HCID 86625228 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Ethyl cyanomethyl(1-(2-nitrophenyl)ethyl)carbamate | HCID 86625229 | 4% |
반응 단계
Preparation of ethyl cyanomethyl(1-(2-nitrophenylethyl)carbamate (19): To the acetonitrile solution containing 2-(1-(2-nitrophenyl)ethylamino)acetonitrile (18) from the previous step was added saturated NaHCO3 (5 mL) and ethyl chloroformate (1.83 g, 16.86 mmol). The reaction mixture was stirred vigorously at room temperature for 14 hours. The reaction was diluted with EtOAc (50 mL) and washed with brine (40 mL). The separated organic phase was dried over Na2SO4, filtered, and concentrated. Purification (Biotage 40 s, 3:1 CH2Cl2:hexanes, then 100% CH2Cl2) provided 37.1 mg (0.134 mmol, 4% yield) of ethyl cyanomethyl(1-(2-nitrophenyl)ethyl)carbamate (19) as a light yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08673898B2 |
| 출처 데이터셋 | uspto-grants-2014_03 |
| ORD ID | ord-adddfb23df0f4c1a882db0c1f4b68a7f |
| 출처 메모 | uspto-grants-2014_03 |