Welcome to chemicalbook!
Chinese English Japanese Germany Korea
010-86108875
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!

101869-74-3

4-methoxyCyclohexanemethanol synthesis

6synthesis methods
95233-12-8 Synthesis
4-METHOXYCYCLOHEXANECARBOXYLIC ACID

95233-12-8
65 suppliers
$30.00/250mg

4-methoxyCyclohexanemethanol

101869-74-3
13 suppliers
inquiry

-

Yield:101869-74-3 91%

Reaction Conditions:

with lithium aluminium tetrahydride in tetrahydrofuran at 0 - 20; for 4 h;Inert atmosphere;

Steps:

18.2 (4-Methoxycyclohexyl)methanol

Lithium aluminum hydride (92.8 mg, 2.45 mmol) was slowly added into the tetrahydrofuran (7 mL) containing methyl-4-methoxycyclohexanecarboxylic acid (280 mg, 1.63 mmol) at 0° C. under the protection of nitrogen.
The reaction solution was stirred at room temperature for 4 hours, and then cooled to 0° C. in an ice-water bath.
Water (0.1 mL), 15% sodium hydroxide (0.1 mL) and water (0.3 mL) was slowly added successively.
The reaction solution was heated to room temperature, and then stirred for half an hour, followed by filtration.
The filter cake was washed with tetrahydrofuran (8 mL*2) and the filtrate was concentrated under reduced pressure to give (4-methoxycyclohexyl)methanol (213 mg, yellow oily) with a yield of 91%. 1H NMR: (400 MHz, Methonal-d4) δ3.49-3.45 (m, 1H), 3.39-3.37 (m, 2H), 3.32 (s, 3H), 1.95-1.80 (m, 3H), 1.56-1.48 (m, 4H), 1.36-1.27 (m, 2H).

References:

US2018/148451,2018,A1 Location in patent:Paragraph 0195; 0198