ChemicalBook CAS DataBase List 5-TERT-BUTYL-2-METHOXYBENZENEBORONIC ACID

5-TERT-BUTYL-2-METHOXYBENZENEBORONIC ACID synthesis

6synthesis methods

Product Name:5-TERT-BUTYL-2-METHOXYBENZENEBORONIC ACID
CAS Number:128733-85-7
Molecular formula:C11H17BO3
Molecular Weight:208.06

5419-55-6
376 suppliers
$12.00/5g

41280-65-3 Synthesis

41280-65-3
36 suppliers
$130.00/500mg

5-TERT-BUTYL-2-METHOXYBENZENEBORONIC ACID

128733-85-7
59 suppliers
$28.00/100mg

Yield: 74%

Reaction Conditions:

with n-butyllithium in tetrahydrofuran;hexane at -78 - 0; for 4.5 h;Inert atmosphere;

Steps:

5.2 (5-(tert-Butyl)-2-methoxyphenyl)boronic acid
n-Butyllithium in hexane (2.5 M, 18.1 mL, 45.24 mmol) was added dropwise to a solution of 2-bromo-4-(tert-butyl)-1-methoxybenzene (10.0 g, 41.13 mmol) and triisopropyl borate (11.39 mL, 49.35 mmol) in tetrahydrofuran (90 mL) at -78° C. under nitrogen.
The reaction mixture was stirred at -78° C. for 3 hours then allowed to warm slowly to 0° C. over 90 minutes.
The reaction was then quenched by the addition of water (90 mL) and the tetrahydrofuran removed under reduced pressure.
The resulting aqueous suspension was partitioned between diethyl ether (80 mL) and 1.0 M aqueous sodium hydroxide solution (100 mL).
The aqueous phase was separated, cooled to 0° C. then acidified to pH 1 by the addition of concentrated hydrochloric acid.
The resulting white suspension was stood at 0° C. for 15 minutes then filtered washing the solid product with water and cold hexane to give (5-(tert-butyl)-2-methoxyphenyl)boronic acid (6.349 g, 74% yield) as a white crystalline solid.
HPLC/MS R_t=5.04 min, m/z 209.1 (M+H⁺).

References:

Jacobus Pharmaceutical Company, Inc.;Heffernan, Gavin David;Jacobus, David Penman;Saionz, Kurt William;Schiehser, Guy Alan;Shieh, Hong-Ming;Zhao, Wenyi US2014/135320, 2014, A1 Location in patent:Paragraph 0241; 0242