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2-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethanol synthesis

3synthesis methods
269410-28-8 Synthesis
4-(ETHOXYCARBONYL)METHOXYPHENYLBORONIC ACID

269410-28-8
44 suppliers
$50.00/100mg

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Yield: 93%

Reaction Conditions:

with sodium tetrahydroborate;ethanol in tetrahydrofuran at 20; for 2 h;Cooling with ice;

Steps:

B Step B:
Step B:
methyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanol
To a solution of ethyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetate (1 g, 3.27 mmol) in tetrahydrofuran/ethanol (10 mL/10 mL) was added sodium borohydride (124 mg, 3.27 mmol) under ice-water bath.
The mixture was allowed to warm to room temperature and stirred for 2 hours.
The mixture was partitioned between ethyl acetate (100 mL) and water (50 mL).
The organic layer was separated, washed with brine (20 mL*3), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to give methyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanol (0.8 g, 93%) as colorless oil.

References:

Arvinas, Inc.;Yale University;Crew, Andrew P.;Hornberger, Keith R.;Wang, Jing;Dong, Hanqing;Qian, Yimin;Crews, Craig M.;Jaime-Figueroa, Saul US2018/179183, 2018, A1 Location in patent:Paragraph 1383