Thionyl Chloride → HCID 58814754, compound

HRID 544792Notes

Reaction equation

HRID 544792 reaction equation
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=O.S(Cl)(Cl)=O.[N:24]12[C:46](=[O:47])[CH2:45][NH:44][CH2:43][C:42](=[O:48])[N:33]([CH2:34][CH2:35][O:36][CH2:37][CH2:38][O:39][CH2:40][CH2:41]1)[CH2:32][CH2:31][O:30][CH2:29][CH2:28][O:27][CH2:26][CH2:25]2.CCN(C(C)C)C(C)C>C(Cl)Cl.CO>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([N:44]1[CH2:45][C:46](=[O:47])[N:24]2[CH2:25][CH2:26][O:27][CH2:28][CH2:29][O:30][CH2:31][CH2:32][N:33]([CH2:34][CH2:35][O:36][CH2:37][CH2:38][O:39][CH2:40][CH2:41]2)[C:42](=[O:48])[CH2:43]1)=[O:19]

Participants

6

Reactant 4

HCID 24386Thionyl ChlorideHCID 81531DiisopropylethylamineHCID 62039716-Bromohexadecanoic acidHCID 179954354,7,13,16-Tetraoxa-1,10,21-triazabicyclo[8.8.5]tricosane-19,23-dione

Product 1

HCID 58814754HCID 58814754, compound

Reagents, catalysts & solvents 1

HCID 21226129Dichloromethane methanolSolvent

Procedure

In a round bottom flask, 0.99 g (3 mmol) of 16-bromohexadecanoic acid was dissolved in 15 mL (15 mmol) of thionyl chloride. The solution was heated at reflux for 30 minutes. Thionyl chloride was removed under reduced pressure, at 40° C. The residue was dissolved in 30 mL of dichloromethane. To this solution, 1.11 g (3.1 mmol) of 4,7,13,16-tetraoxa-1,10,21-triaza-bicyclo[8.8.5]tricosane-19,23-dione and 1.4 mL (7.7 mmol) of DIPEA were added. The mixture was stirred at room temperature for 1 day. DIPEA and solvent were removed from the solution by evaporation of the solvent mixture under reduced pressure, and the residue was redissolved in 100 mL of dichloromethane. The solution was washed three times with 100 mL of 2 N HCl, once with 100 mL of water, and finally dried over anhydrous MgSO4. The solvent was removed under reduced pressure and the product was finally purified by column chromatography (CH2Cl2:CH3OH 20:1) to afford a yellow oil. Yield: 0.96 g (72%). Rf:0.32 (CH2Cl2:CH3OH 20:1), 1H-NMR (400 MHz, CDCl3): δ 1.24-1.42 (m, 22H), 1.65-1.67 (m, 2H), 1.82-1.89 (m, 2H), 2.38-2.42 (dd, J=15.41, 7.58 Hz, 2H), 2.66-2.83 (m, 2H), 2.97-3.05 (m, 2H), 3.41 (t, J=6.82, 2H), 3.47-3.72 (m, 16H), 3.82-3.99 (m, 4H), 4.22-4.40 (m, 4H). 13C-NMR (100 MHz, CDCl3): δ 25.5 (CH2), 28.5 (CH2), 29.1 (CH2), 29.8 (CH2), 29.8 (CH2), 29.9 (CH2), 30.0 (CH2), 33.1 (CH2), 33.2 (CH2), 34.5 (CH2), 45.8 (CH2), 48.7 (CH2), 49.6 (CH2), 50.3 (CH2), 50.8 (CH2), 50.8 (CH2), 67.3 (CH2), 67.8 (CH2), 70.3 (CH2), 70.9 (CH2), 71.1 (CH2), 71.3 (CH2), 71.8 (CH2), 72.6 (CH2), 168.9 (C═O), 169.5 (C═O), 174.5 (C═O).

Workup

  1. temperatureThe solution was heated
  2. temperatureat reflux for 30 minutes
  3. customThionyl chloride was removed under reduced pressure, at 40° C
  4. dissolutionThe residue was dissolved in 30 mL of dichloromethane
  5. customDIPEA and solvent were removed from the solution by evaporation of the solvent mixture under reduced pressure
  6. dissolutionthe residue was redissolved in 100 mL of dichloromethane
  7. washThe solution was washed three times with 100 mL of 2 N HCl
  8. dry with materialonce with 100 mL of water, and finally dried over anhydrous MgSO4
  9. customThe solvent was removed under reduced pressure
  10. customthe product was finally purified by column chromatography (CH2Cl2:CH3OH 20:1)
  11. customto afford a yellow oil

Sources & evidence

ORD record
ord-e2d9bed5c3154c81a0f5285af716e8e6
Source dataset
uspto-grants-2011_05
Patent number
US07935309B2

Reaction notes

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