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氟噻草胺的合成 被引量:16

Synthesis of a New Herbicide Flufenact
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摘要 本文介绍氟噻草胺合成工艺,以水合肼、三氟乙酸为原料合成2-甲砜基-5-三氟甲基-1,3,4-噻二唑;以对氟硝基苯、丙酮经过催化加氢、酰化、醇解合成N-(4-氟苯基[(\))0(-)]N-异丙基-2-羟甲基乙酰胺;及氟噻草胺的制备。 The article described the synthesis of flufenact,a herbicide. It抯 achieved via condensation of interediates, 2-methylsulfonyl-5-trifluoromethyl-1,3,4thiadiazol and N-(4-fluorophenyl)-2-hydroxy-N-(1-methylethyl)acetamide. The former intermediate is prepared starting from hydrazine hydrate and trifluroracetic acid. The latter is obtained by using 4-nitro-fluorobenzene and acetone as starting materials through a series of reaction, such as catalytic hydrogenation, alcoholysis and amidation.
出处 《现代农药》 CAS 2002年第2期8-10,共3页 MODERN AGROCHEMICALS
关键词 合成路线 制备 水合肼 三氟乙酸 除草剂 flufenact, synthesie, route, preparation
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  • 1[1]John J.Damico; Frederic G.Bollinger et al.Synthesisof 3a,4,5,6,7a- hexahydro-3a-hydroxy-3-substitutedamino-2-benzathiaiolin ethiones and Related Compounds[1] J.Heter.chem.1986,23 ①: 105~12
  • 2[2]Hamberger Helmut,FliriHans..et al.(Sandoz Ltd.).DE 3223019 .1983
  • 3[3]Diehr,Hans-joachim dr.(Bayer AG).DE 3709414 1990
  • 4[4]Newman Howard; Tomcufcik Andrew Stephen et al.(American Cyanamid Co.).US 3562284 1971
  • 5[5]Diehr Hans-Joachim et al .(Bayer AG).DE 4003436 .1992
  • 6[6]Nusslein Ludwig et al .(Schering AG).US 4061645 .1977
  • 7[7]Maurer Fritz Dr nibon et al.(Bayer AG).DE 4003078.1992
  • 8[8]Rohe Cothar et al .(Bayer AG).US 5817876.1998
  • 9[9]Vidyanatha A.prasad et al .(Bayer AG).US 5808153.1997
  • 10[10]Planker Siegfied et al.(Hoechst AG).EP 678502.1997

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