反応式
[CH3:1][C:2]1([CH3:19])[CH:4]([CH:5]=[C:6]([Cl:8])[Cl:7])[C:3]1(C(OCC)=O)[C:9]([O:11][CH2:12][CH3:13])=[O:10].N12CCCC1=NCCC2>CC1C=CC=CC=1C>[CH2:12]([O:11][C:9]([CH:3]1[CH:4]([CH:5]=[C:6]([Cl:7])[Cl:8])[C:2]1([CH3:1])[CH3:19])=[O:10])[CH3:13]参加物
実験手順
13 g of diethyl 2,2-dimethyl-3-(2',2'-dichlorovinyl)-cyclopropane-1,1-dicarboxylate were dissolved in 50 g of o-xylene and 20 g of 1,5-diaza-bicyclo[4.3.0]non-5-ene were added. The mixture was then heated to the boil for 8 hours. After cooling, ice-cold dilute hydrochloric acid was added, so that a neutral or weakly acid pH value resulted. The organic phase was separated off and dried with Na2SO4 and the xylene was distilled off in vacuo (boiling point = 35° - 40° C./12 mm Hg). The residue weighed 12.5 g. Fractional distillation gave 4.7 g of 2,2-dimethyl-3-(2',2'-dichlorovinyl)-cyclopropane-1-carboxylic acid ethyl ester, of which 30% was in the cis form and 70% was in the trans form. The boiling point was 65° - 72° C./0.3 mm Hg. The nuclear magnetic resonance spectrum agreed with that given in the literature. 6.5 g of the starting material were recovered. The yield was thus 92%.
後処理
- temperatureThe mixture was then heated to the boil for 8 hours
- temperatureAfter cooling
- additionice-cold dilute hydrochloric acid was added
- customresulted
- customThe organic phase was separated off
- dry with materialdried with Na2SO4
- distillationthe xylene was distilled off in vacuo (boiling point = 35° - 40° C./12 mm Hg)
- distillationFractional distillation
出典と根拠
- ORDレコード
- ord-78e28cdd9aae484aba09ec936786bc3d
- 出典データセット
- uspto-grants-1978_09
- 特許番号
- US04113969
関連ノート
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