With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.81156-68-5, name is 2,4-Dichlorophenethyl alcohol, molecular formula is C8H8Cl2O, molecular weight is 191.06, as common compound, the synthetic route is as follows.Recommanded Product: 2,4-Dichlorophenethyl alcohol
Example 5 Preparation of methyl 2- [4- (2-F2. 4-DICHLOROPHENYL) ETHOXY) PHENYL- THIO]ISOBUTYRATE (ST2531) The title product was prepared according to the procedure described in Method B starting from methyl 2- (4- hydroxyphenylthio) iso-butyrate (prepared as described in example 3) (0.280 g, 1.24 mmol) and DIAD (0. 325 g, 1.61 mmol) dissolved in 3 mL of anhydrous THF and added dropwise to a solution of 2,4- dichlorophenetylalcohol (0.260 g, 1.36 mmol) and triphenylphosphine (0.422 g, 1.61 mmol) in 4 mL of anhydrous THF at 0C. The reaction was left overnight under magnetic stirring at room temperature After this period, the solvent was evaporated and the residue purified by silica gel chromatography using HEXANE/ACOET 9.6/0. 4 as eluent. 0.346 g of product were obtained (yield: 70%); Mp: 73-74C ; TLC: silica gel, eluent hexane/AcOEt 9/1, Fr: 0.26 ; 1H NMR (CDCIs, 300 MHz) B : 7.35 (m, 3H), 7.22 (m, 2H), 6.83 (d, 2H), 4.18 (t, 2H), 3.65 (s, 3H), 3.20 (t, 2H), 1.45 (s, 6H); HPLC: Column: Inertisil ODS-3 (5, UM) 4.6 x 250 mm, T: room temperature, mobile phase CH3CN/H20 85/15 (v/v), pH: as is, flow rate: 1 mL/min, 205 nm UV detector, retention time 12.58 min; KF: 0.4 % H20 ; E. A. conforming for CL9H20CL203S.
At the same time, in my other blogs, there are other synthetic methods of this type of compound,81156-68-5, 2,4-Dichlorophenethyl alcohol, and friends who are interested can also refer to it.
Reference:
Patent; SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.p.A.; WO2004/56355; (2004); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts