Methyl Laurate → 3-Dimethylaminopropyl Laurate

HRID 1048638

반응식

HRID 1048638 반응식
[C:1]([O:14][CH3:15])(=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH3:16][N:17]([CH:19](O)[CH2:20]CC)[CH3:18]>>[C:1]([O:14][CH2:15][CH2:20][CH2:19][N:17]([CH3:18])[CH3:16])(=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

참가 물질

3

실험 절차

To a 50-mL conical bottom plastic vial was added methyl laurate (38.5 mmol), dimethylaminobutanol (46.2 mmol, 1.2 eq), and Novozym 435 (400 mg). A syringe was inserted through the cap and two additional holes were punched for gas to exit. Nitrogen was bubbled at a rate sufficient to mix the contents. The vial was placed in a heating block set to 65° C. The reaction was monitored by GC/MS to observe the disappearance of starting material. The reaction was complete after approximately 24 hours. The reaction mixture was allowed to cool. The Novozym 435 was removed by filtration to afford the product as a pale, yellow oil (9.2 g; 67% yield) without further purification.

후처리

  1. customA syringe was inserted
  2. customthrough the cap
  3. customNitrogen was bubbled at a rate sufficient
  4. additionto mix the contents
  5. customset to 65° C
  6. temperatureto cool
  7. customThe Novozym 435 was removed by filtration
  8. customto afford the product as a pale, yellow oil (9.2 g; 67% yield)
  9. customwithout further purification

출처 및 근거

ORD 기록
ord-bfabc186a21b4ca28f4e67f89d44ad30
출처 데이터셋
uspto-grants-2016_07
특허 번호
US09381147B2

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