Réaction #1483092

ord-4c1654e980a9489dae21b317a1123de2

Équation de réaction

CCCCCCCCCCCCOC(=O)C(C)N(C)C
DDAIP
CCCCCCCCCCCCOC(=O)C(C)N(C)C
4
CCCCCCCCCCCCOC(=O)C(C)N(C)C
dodecyl 2-(dimethylamino)propanoate
O=S(=O)(O)c1cccc2c(S(=O)(=O)O)cccc12
1,5-napthalene disulfonic acid
CCCCCCCCCCCCOC(=O)C(C)N(C)C.O=S(=O)(O)c1cccc2c(S(=O)(=O)O)cccc12
dodecyl 2-(dimethylamino)propanoate 1,5-napthalene disulfonate salt
Rendement 92.3%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONAfter addition the temperature of the reaction mixture
  2. 2
    ConcentrationThe reaction mixture was concentrated under vacuum
  3. 3
    Autreflushed with ethyl acetate (2×30 mL)
  4. 4
    workup.STIRRINGstirred at RT for ½ h (sticky solid)
  5. 5
    ConcentrationThe reaction mixture was concentrated under vacuum
  6. 6
    Autreflushed with hexane (3×100 mL)

Mode opératoire

A stirred solution of DDAIP base 4 (80 g, 280 mmol) in methanol (500 mL) was cooled to 0° C., then 1,5-napthalene disulfonic acid 22 (50.5 g, 140 mmol) was added in one lot. After addition the temperature of the reaction mixture was slowly raised to RT and stirred at RT for 72 h; the reaction mixture was monitored by TLC. The reaction mixture was concentrated under vacuum and flushed with ethyl acetate (2×30 mL). The obtained residue was taken in n-hexane (200 mL) and stirred at RT for ½ h (sticky solid). The reaction mixture was concentrated under vacuum and flushed with hexane (3×100 mL) to afford dodecyl 2-(dimethylamino)propanoate 1,5-napthalene disulfonate salt (23, Nex-32) (120 g, 92.3%) as a white solid. Mp: 135-140° C. 1H-NMR (400 MHz, CDCl3): δ 0.9 (t, 3H), 1.2-1.3 (m, 18H), 1.6 (d, 3H), 1.65 (q, 2H), 2.9 (s, 6H), 4.15 (t, 2H), 4.2 (q, 1H), 7.55 (t, 2H), 8.22 (d, 2H), 9.1 (d, 2H); LCMS: 286 (M++1); HPLC: 80.48%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08900625B2uspto-grants-2014_12