Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 4-tert-Amylphenol

4-tert-Amylphenol synthesis

13synthesis methods
-

Yield:80-46-6 93%

Reaction Conditions:

Stage #1: 1-allyloxy-4-(1',1''-dimethylpropyl)benzenewith C12H37NiP4(1+)*C2F6NO4S2(1-) in tetrahydrofuran at 20; for 0.5 h;Glovebox;Schlenk technique;Inert atmosphere;
Stage #2: with toluene-4-sulfonic acid in tetrahydrofuran; for 15 h;Glovebox;Schlenk technique;Reflux;Inert atmosphere;

Steps:

Procedure C: Catalysis

General procedure: Inside a glovebox, a flame-dried 15 mL Schlenk tube was charged with [Ni(PMe3)4H](SO2CF3)2N (1.6 mg,2.48 μmol, 1 mol-%), and dry THF was added (0.16 M, 1.5 mL) using a Schlenk line. The O-allyl ether(0.25 mmol, 1 equiv) was then added under argon counter-flow. The reaction mixture was allowed to stirat room temperature for 30 minutes. This was followed by addition of pTsOH·H2O (1 equiv) and thereaction mixture was then heated to reflux for the time specified. The reaction was quenched by additionof ethyl acetate and water followed by transfer to a separating funnel. The aqueous phase was extractedwith ethyl acetate (3 × 5 mL), and the combined organic phases were then dried over MgSO4 and dried byrotary evaporation to give the crude alcohol, which was finally purified by column chromatography onsilica gel.

References:

Kathe, Prasad M.;Berkefeld, Andreas;Fleischer, Ivana [Synlett,2021,vol. 32,# 16,p. 1629 - 1632] Location in patent:supporting information

4-tert-Amylphenol Related Search: