Benzaldehyde → 1-Benzyldiethylenetriamine

HRID 1422053

반응식

HRID 1422053 반응식
[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

참가 물질

5

반응물 3

HCID 240BenzaldehydeHCID 8111DiethylenetriamineHCID 4311764Sodium borohydride

생성물 1

HCID 382921-Benzyldiethylenetriamine

시약·촉매·용매 1

HCID 887Methanol용매2회

반응 조건

온도
25 °C

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-53dd929c13764acf83fe76068f2467f5
출처 데이터셋
uspto-grants-2000_06
특허 번호
US06080785

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