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ChemicalBook CAS DataBase List 1-TRITYLIMIDAZOLE-2-CARBOXALDEHYDE
67478-50-6

1-TRITYLIMIDAZOLE-2-CARBOXALDEHYDE synthesis

7synthesis methods
-

Yield:67478-50-6 81%

Reaction Conditions:

Stage #1: 2-imidazolecarbaldehydewith triethylamine in N,N-dimethyl-formamide at 20; for 0.25 h;
Stage #2: trityl chloride in N,N-dimethyl-formamide; for 48 h;

Steps:

5.1.22. 1-Triphenylmethyl-1H-imidazol-2-carbaldehyde (38)

1H-Imidazol-2-carbaldehyde (36) (1.98 g, 20.0 mmol) in DMF (20 mL) was treated with NEt3 (4.10 g, 40.0 mmol, 5.62 mL). The mixture was stirred for 15 min at rt before triphenylmethyl chloride (37) (6.26 g, 22.0 mmol), suspended in DMF (10 mL), was added. After stirring for 48 h the solution was diluted with EtOAc (20 mL/mmol) and washed with brine, sat. Na2CO3-solution and H2O. The organic layers were dried over MgSO4, filtered and concentrated. The crude product was purified by CC (n-Pentane/EtOAc = 6/4).Colourless crystals; Yield: 5.59 g (81%); mp 190 °C. IR (KBr) ν cm-1: 3397, 3065, 2845, 1708, 1491, 1442, 1396, 1356, 1242, 1169; 500 MHz 1H NMR (CD3OD): δ = 7.01 (s, 1H, CH[5H-Imid.]), 7.09-7.11 (m, 6H, CHar), 7.24-7.36 (m, 10H, CHar, CH[4H-Imid.]), 9.21 (s, 1H, CHO); 126 MHz 13C NMR (CDCl3): δ = 76.9 (C(C6H5)3), 126.9 (CHar), 128.1 (CHar), 129.6 (CH[4C-Imid.], CH[5C-Imid.]), 142.1 (C[2C-Imid.]), 145.6 (Cq), 178.6 (CHO); MS (CI, CH5+): m/z (%) = 338 (1) [M++1], 243 (100), 167 (109); MS (FAB, NBA): m/z (%) = 339.2 (5) [M++1], 243.2 (100), 165.1 (11); HMRS (ESI) calcd. for C23H18N2ONa1: 361.1317; found 361.1313.

References:

Hack, Silke;W?rlein, Babette;H?fner, Georg;Pabel, J?rg;Wanner, Klaus T. [European Journal of Medicinal Chemistry,2011,vol. 46,# 5,p. 1483 - 1498] Location in patent:experimental part

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