1,5-Diazabicyclo(4.3.0)non-5-ene → Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, ethyl ester

HRID 1763955

反応式

HRID 1763955 の反応式
[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

4

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

  1. temperatureThe mixture was then heated to the boil for 8 hours
  2. temperatureAfter cooling
  3. additionice-cold dilute hydrochloric acid was added
  4. customresulted
  5. customThe organic phase was separated off
  6. dry with materialdried with Na2SO4
  7. distillationthe xylene was distilled off in vacuo (boiling point = 35° - 40° C./12 mm Hg)
  8. 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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