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Dimethylamine → Ethyl 2-dimethylaminomethylacrylate

HRID 616432
ノート
印刷プレビュー

反応式

HRID 616432 の反応式
[CH2:1]=O.[C:3]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:4][C:5](O)=O.[CH3:12][NH:13][CH3:14]>O>[CH3:12][N:13]([CH2:5][C:4](=[CH2:1])[C:3]([O:9][CH2:10][CH3:11])=[O:8])[CH3:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 674DimethylamineHCID 712FormaldehydeHCID 70615Monoethyl malonate

生成物 1

HCID 20370247Ethyl 2-dimethylaminomethylacrylate収率 32%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
15 °C

実験手順

Aqueous formaldehyde (161 ml, 37%) was added slowly to a solution of ethyl hydrogen malonate (132g) and dimethylamine (350 ml, 26% aqueous) in water (150 ml) at 15° C. The mixture was stirred at 15° C for 30 minutes, heated slowly to 40° C and stirred for a further 30 minutes. Decarboxylation commenced at 26° C. After cooling, the organic material which had separated as a colourless oil was extracted with ether (3 × 250 ml). The ether extracted was dried over anhydrous sodium sulphate and evaporated at atmospheric pressure. The residue was shown to be a mixture by the appearance of two carbonyl peaks (1740 cm-1 and 1720 cm-1) in the infrared spectrum. The mixture was distilled under vacuum to give ethyl 2-dimethylaminomethylacrylate (50g, 32% boiling point 34° C/0.7mm; νc=o 1722cm-1) and ethyl 1,3-bis (dimethylamino) propane-2-carboxylate (87g, 43%, boiling point 58° C/0. 8mm;νc=o 1740 cm-1).

後処理

  1. temperatureheated slowly to 40° C
  2. stirringstirred for a further 30 minutes
  3. customcommenced at 26° C
  4. temperatureAfter cooling
  5. customthe organic material which had separated as a colourless oil
  6. extractionwas extracted with ether (3 × 250 ml)
  7. extractionThe ether extracted
  8. dry with materialwas dried over anhydrous sodium sulphate
  9. customevaporated at atmospheric pressure
  10. distillationThe mixture was distilled under vacuum

出典と根拠

ORDレコード
ord-f19bd4b6e24a460285eeb33517ba8fa1
出典データセット
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04074051

反応ノート

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