Discovery of 3344-70-5

According to the analysis of related databases, 3344-70-5, the application of this compound in the production field has become more and more popular.

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 3344-70-5, name is 1,12-Dibromododecane, This compound has unique chemical properties. The synthetic route is as follows., HPLC of Formula: C12H24Br2

Example 11 (n=12); (a) 1,1′-[(Dodecane-1,12-diyl)dioxy]bis[(11S,11aS)-10-(tert- butyloxycarbonyl)-8-methoxy-11- (tetrahydro-pyran-2-yloxy)- 1, 2, 3, 10, 11, 11a-hexahydro-5H-pyrrolo[2,1-c][1,4]benzodiazpeine-5- one] (8j); 1,12-Dibromododecane (73.1 mg, 0.22 mmol, 0.5 equiv) was added to the mixture of monomer 7 (0. 2 g, 0.44 mmol, 1.0 equiv) potassium carbonate (0.98 mmol, 2. 2 equiv) and a catalytic amount of potassium iodide in dry DMF (30 mL), and the resulting mixture was heated to 90°C under a nitrogen atmosphere for 5 h. Removal of excess solvent under reduced pressure afforded a crude solid, which was subjected to flash column chromatography (SiO2, 50percent EtOAc- hexane) to afford the dimerized compound 8j (208 mg, 0.19 mmol, 87percent yield, mixture of diastereomers from THP protecting group) as a solid: [alpha]20D = +50° (c = 0.20, CHC13) ; 1H NMR (CDCl3, 400 MHz): No. 1.26-1. 68 (m, 84H, 14-H, 15-H, 16-H, 17-H, Boc, THP), 1.69-1. 89 (16H, 13-H, THP), 1.93-2. 20 (m, 16H, 1-H, 2-H), 3.44-3. 75 (m, 16H, 3-H, lla-H, THP), 3.83-4. 14 (m, 24H, 12-H, 7-OMe, THP), 5.02-5. 10 (m, 2H, THP), 5.12-5. 19 (m, 2H, THP), 5.69-5. 77 (d, 2H, 11-H), 5.79-5. 89 (d, 2H, 11-H), 6.50 (s, 2H, 9-H), 6.87 (s, 2H, 9-H), 7.19 (s, 2H, 6-H), 7.22 (s, 2H, 6-H) ;”C NMR (CDCl3, 400 MHz): 5 19.9, 20.4, 23.1, 23.2, 25.2, 25.3, 25.9, 28.1, 28.2, 28.9, 29.0, 29.1, 29.2, 29.3, 29.56, 29.58, 30.9, 31.2, 46.2, 55.9, 56.2, 60.0, 60.1, 63.3, 64.4, 69.12, 69.15, 80. 9,81. 2,88. 2,91. 2, 95.8, 100.2, 111.1, 111.5, 113.4, 114.0, 126.3, 129.6, 134. 1, 138.8, 147.8, 148.1, 151.5, 155.3, 167.4, 167.6 ; IR (neat): 2932, 1703,1643, 1604,1513, 1450,1392, 1327,1218, 1164, 1022cm~1 ; MS (FAB) m/z (relative intensity) 1085 ( + Na] +, 28), 1063 (M 100), 961 (17), 861 (13).

According to the analysis of related databases, 3344-70-5, the application of this compound in the production field has become more and more popular.

Reference:
Patent; SPIROGEN LIMITED; WO2005/85259; (2005); A2;,
Bromide – Wikipedia,
bromide – Wiktionary