Reacción #1483092

ord-4c1654e980a9489dae21b317a1123de2

Ecuación de reacción

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
Rendimiento 92.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08900625B2uspto-grants-2014_12