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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

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참여 물질

역할이름HCID투입량
반응물CarbofuranHCID 2566—
반응물TriethylamineHCID 8471—
반응물Sulfur dichlorideHCID 25353—
반응물Ethyl 2-(butylamino)acetateHCID 10607047—
용매DichloromethaneHCID 6344—
생성물Glycine, N-butyl-N-(((((2,3-dihydro-2,2-dimethyl-7-benzofuranyl)oxy)carbonyl)methylamino)thio)-, ethyl esterHCID 3067959—

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04413005
출처 데이터셋uspto-grants-1983_11
ORD IDord-5b912645e49f4132909dbc79a4562a5a
출처 메모uspto-grants-1983_11