Trifluoroacetic acid → N-Fmoc,2-(trans-Dec-4-en-1-ylamino)acetaldehyde

HRID 1282271Notes

Reaction equation

HRID 1282271 reaction equation
C[O:2][CH:3](OC)[CH2:4][N:5]([CH2:23][CH2:24][CH2:25]/[CH:26]=[CH:27]/[CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[C:6]([O:8][CH2:9][CH:10]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[C:16]2[C:11]1=[CH:12][CH:13]=[CH:14][CH:15]=2)=[O:7].C(O)(C(F)(F)F)=O>O>[C:6]([N:5]([CH2:23][CH2:24][CH2:25]/[CH:26]=[CH:27]/[CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:4][CH:3]=[O:2])([O:8][CH2:9][CH:10]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[C:16]2[C:11]1=[CH:12][CH:13]=[CH:14][CH:15]=2)=[O:7]

Participants

4

Procedure

N-Fmoc-2-(trans-Dec-4-en-1-ylamino)acetaldehyde dimethyl acetal (5 g, 10.7 mmol) was mixed with 30 mL of TFA and stirred at room temperature for 30 minutes. The reaction was poured into water (140 mL) and centrifuged to obtain a clear oil. The supernatant was decanted and the oil was mixed with 40 mL of water and centrifuged again. The supernatant was again decanted and the oil was dissolved in dichloromethane (100 mL), dried over MgSO4, filtered, and concentrated under reduced pressure to obtain 5.2 g (12.3 mmol) of N-Fmoc-2-(trans-Dec-4-en-1-ylamino)acetaldehyde as a clear oil.

Workup

  1. customto obtain a clear oil
  2. customThe supernatant was decanted
  3. additionthe oil was mixed with 40 mL of water
  4. customThe supernatant was again decanted
  5. dissolutionthe oil was dissolved in dichloromethane (100 mL)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-c4cae7a8cba340e984eacaede95bc475
Source dataset
uspto-grants-2002_09
Patent number
US06455669B1

Reaction notes

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