تفاعل #40283

ord-aa18151d93744dfa8c50f3a6124f9344

معادلة التفاعل

[Cl-].[Na+]
NaCl
CC1(C)C2CCC1(CS(=O)(=O)O)C(=O)C2
Camphor sulfonic acid
COOC(OOC)c1ccc(OC)cc1
p-anisaldehyde-dimethoxy-acetal
CC(C)(CO)[C@@H](O)C(=O)NCCC(=O)O
Pantothenic acid
COc1ccc(C2OCC(C)(C)C(C(=O)NCCC(=O)O)O2)cc1
3-{[2-(4-Methoxy-phenyl)-5,5-dimethyl-[1,3]dioxane-4-carbonyl]-amino}-propionic acid
المردود 51.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe crude reaction product
  2. 2
    تركيزwas concentrated
  3. 3
    أخرىpurified silica gel chromatography (6:1 hexane:EtOAC-EtOAc)
  4. 4
    أخرىto yield a white solid (8A1) (3.8 g, 51% yield)

الإجراء التجريبي

Pantothenic acid (7) (4.6 g, 2.24×10−2 mols) was dissolved in dry DCM (30 mL). Camphor sulfonic acid (0.52 g, 2.24×10−3 mols) and p-anisaldehyde-dimethoxy-acetal (3.82 mL, 2.24×10−2 mols) were added to the reaction mixture. The reaction was stirred overnight at room temperature with a drying tube. The crude reaction product was concentrated and purified silica gel chromatography (6:1 hexane:EtOAC-EtOAc) to yield a white solid (8A1) (3.8 g, 51% yield). mp=135-136° C. 1HNMR (400 MHz, DMSO) 0.93 (s, 3H), 0.99 (s, 3H), 2.38 (t, 2H, J=6.8 Hz), 3.25 (m, 1H), 3.34 (m, 1H), 3.5.9 (d, 1H, J=10.8 Hz), 3.62 (d, H, J=10.8 Hz), 3.74 (s, 3H), 4.07 (s, 1H), 5.50 (s, 1H), 6.91 (d, 2H, J=8.8 Hz), 7.41 (d, 2H, J=8.8 Hz). 13C-NMR (400 Mz, DMSO) 19.7, 22.2, 33.2, 34.4, 34.9, 55.8, 78.0, 83.8, 101.1, 114.0, 128.4, 131.1, 160.3, 168.9, 173.8. IR (NaCl, thin film), 3420, 2959, 1729, 1654, 1617, 1540, 1520, 1251, 1105 cm−1. MS (ESI) [M+Na]+360.1. HRMS (FAB) (m/z): [M+H]+ calcd for C17H23O6N, 338.1598, found 338.1594.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07727738B2uspto-grants-2010_06