تفاعل #1483088

ord-4fb5b8046f4b428b87b352d894426fd4

معادلة التفاعل

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)c1ccccc1
benzene sulfonic acid
CCCCCCCCCCCCOC(=O)C(C)N(C)C.O=S(=O)(O)c1ccccc1
dodecyl 2-(dimethylamino)propanoate benzene sulfonate salt
المردود 99.5%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    تركيزThe reaction mixture was concentrated under vacuum
  3. 3
    غسيلThe residue washed with hexane (2×30 mL)
  4. 4
    workup.WAITThe obtained sticky solid was kept in deep freezer for 12 h

الإجراء التجريبي

A stirred solution of DDAIP base 4 (75 g, 263 mmol) in ethyl acetate (500 mL) was cooled to 0° C., then benzene sulfonic acid 14 (41.55 g, 263 mmol) was added in one lot. After addition, the temperature of the reaction mixture was slowly raised to RT and stirred at RT for 24 h; the reaction mixture was monitored by TLC. The reaction mixture was concentrated under vacuum. The residue washed with hexane (2×30 mL); after workup a sticky solid was observed. The obtained sticky solid was kept in deep freezer for 12 h to afford dodecyl 2-(dimethylamino)propanoate benzene sulfonate salt (15, Nex-16) (116 g, yield: 99.5%) as a solid, mp: 55-62° C. 1H-NMR (400 MHz, CDCl3): δ 0.9 (t, 3H), 1.3 (m, 18H), 1.65 (d, 3H), 1.65 (q, 2H), 3 (s, 6H), 4.2 (q, 1H), 4.2 (t, 2H), 7.4 (m, 3H), 7.9 (d, 2H); LCMS: 286 (M++1); HPLC: 80.48%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08900625B2uspto-grants-2014_12