Benzaldehyde → 1-Benzyldiethylenetriamine

HRID 1422053

反応式

HRID 1422053 の反応式
[NH2:1][CH2:2][CH2:3][NH:4][CH2:5][CH2:6][NH2:7].[CH:8](=O)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[BH4-].[Na+]>CO>[CH2:8]([NH:1][CH2:2][CH2:3][NH:4][CH2:5][CH2:6][NH2:7])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1

参加物

5

反応条件

温度
25 °C

実験手順

A stirred solution of 108.26 ml (998 mmol) of 1,4,7-triaza-heptane in 750 absolute methanol is mixed at 0° C. drop by drop with a solution of 20.0 g (188 mmol) of benzaldehyde in 100 ml of absolute methanol. After a reaction time of 2 hours at 0° C., it is mixed in portions with a total of 7.13 g (188 mmol) of sodium borohydride and stirred for another 12 hours at 25° C. For working-up, the reaction mixture is filtered on diatomaceous earth, and the solvent is drawn off in a vacuum. The remaining oily residue is mixed with dichloromethane (250 ml) and water (250 ml) and extracted. After extraction of the aqueous phase is again performed with dichloromethane, the combined organic phases are dried on sodium sulfate, filtered, and the solvent is drawn off in a vacuum. The residue is chromatographed on silica gel (eluant: methanol/aqueous ammonia solution 20/1).

後処理

  1. filtrationthe reaction mixture is filtered on diatomaceous earth
  2. additionThe remaining oily residue is mixed with dichloromethane (250 ml) and water (250 ml)
  3. extractionextracted
  4. extractionAfter extraction of the aqueous phase
  5. customthe combined organic phases are dried on sodium sulfate
  6. filtrationfiltered
  7. customThe residue is chromatographed on silica gel (eluant: methanol/aqueous ammonia solution 20/1)

出典と根拠

ORDレコード
ord-53dd929c13764acf83fe76068f2467f5
出典データセット
uspto-grants-2000_06
特許番号
US06080785

関連ノート

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