Propanedioic acid, monoethyl ester → Propanedioic acid, monoethyl ester

HRID 2419814ノート

反応式

HRID 2419814 の反応式
[Mg:1].[C:2]([O:8][CH2:9][CH3:10])(=[O:7])[CH2:3][C:4]([O-:6])=[O:5]>>[CH2:2]([O:8][Mg:1])[CH3:3].[C:2]([O:8][CH2:9][CH3:10])(=[O:7])[CH2:3][C:4]([O-:6])=[O:5]

参加物

4

実験手順

Using the procedure of Step C of Example 6, 1.34 g of magnesium and 8.8g of ethyl malonate were reacted to obtain ethoxy magnesium of ethyl malonate to which was added over 30 minutes at room temperature a solution of 12.4 g of the product of Step B in 10 ml of dry toluene. The mixture was held at room temperature for 45 minutes and was then poured into 50 ml of 2N hydrochloric acid and 50 ml of ice. The mixture was extracted with ether and the extracts were washed with 5% sodium bicarbonate solution and then with water until the wash water pH was 6. The extracts were dried over magnesium sulfate, treated with activated carbon and evaporated to obtain 18 g of ethyl 2-[1-(2-trifluoromethylphenylamino)-2-methyl-prop-1-ylidene]-propanedioate in the form of a yellow oil which was used as is for the next step.

後処理

  1. customwere reacted

出典と根拠

ORDレコード
ord-7ae7fa58560d46b78b0292ed9f8329c2
出典データセット
uspto-grants-1978_08
特許番号
US04107310

反応ノート

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