Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1648758생성일: 2026년 10월 26일
Carbofuran → Glycine, N-butyl-N-(((((2,3-dihydro-2,2-dimethyl-7-benzofuranyl)oxy)carbonyl)methylamino)thio)-, ethyl ester
https://huagongshe.com/reaction/1648758
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbofuran | HCID 2566 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Sulfur dichloride | HCID 25353 | — |
| 반응물 | Ethyl 2-(butylamino)acetate | HCID 10607047 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Glycine, N-butyl-N-(((((2,3-dihydro-2,2-dimethyl-7-benzofuranyl)oxy)carbonyl)methylamino)thio)-, ethyl ester | HCID 3067959 | — |
반응 단계
A 11 g quantity (0.05 mole) of 2,3-dihydro-2,2-dimethylbenzofuran-7-yl N-methyl-carbamate was dissolved in 70 ml of methylene chloride, 5.2 g (0.05 mole) of sulfur dichloride was added to the solution with cooling, and 5 g (0.05 mole) of triethylamine was further added dropwise to the solution at -10° to -5° C. The mixture was stirred at 0° C. for one hour and further at room temperature for 2 hours. After cooling to -10° to -5° C., 8.0 g (0.05 mole) of N-butylglycine ethyl ester was added dropwise to the mixture, and 5 g (0.05 mole) of triethylamine was further added dropwise to the mixture. The resulting mixture was stirred at 0° C. for 2 hours and thereafter allowed to stand overnight at room temperature. With addition of 100 ml of methylene chloride, the reaction mixture was washed with 100 ml of water three times. The methylene chloride layer was dried and then concentrated in a vacuum to give an oily product, which was almost entirely composed of the desired product although containing small amounts of impurities. Yield: 15.7 g (76.6%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04413005 |
|---|
| 출처 데이터셋 | uspto-grants-1983_11 |
|---|
| ORD ID | ord-5b912645e49f4132909dbc79a4562a5a |
|---|
| 출처 메모 | uspto-grants-1983_11 |
|---|