KR20120109928A - Novel synthesis of alcohol derivatives using indium - Google Patents

Abstract

PURPOSE: A manufacturing method of alcohol derivative is provided to reduce a use amount of metal, to obtain high yield at room temperature in short time, and to be suitable for manufacturing alcohol for medicine and perfume by using environmental-friendly isopropanol as a solvent and indium which has less toxicity as solvents. CONSTITUTION: A manufacturing method of alcohol derivative comprises: a step of preparing an alcohol derivative in chemical formula 1 by reacting an aldehyde derivative in chemical formula 2 and an indium alkoxide derivative in chemical formula 3. In chemical formula 1-3, R is (C1-C10)alkyl, (C3-C12) cycloalkyl, (C6-C12) aryl, (C3-C12)heteroaryl, a functional group in chemical formula (a) or a functional group in chemical formula (b), R^11-R^15 is independently hydrogen, halogen, (C1-C10)alkyl or (C3-C12)aryl, and R^1 and R^2 is (C1-C10)alkyl.

Description

Method for preparing alcohol derivative using indium {Novel synthesis of alcohol derivatives using indium}

The present invention relates to a method for producing an alcohol derivative using indium. More specifically, the present invention relates to a method of preparing an alcohol derivative through a Meerwein-Ponndorf-Verley (MPV) reduction reaction of an aldehyde derivative using an organoindium reagent.

Alcohol is an organic compound containing hydroxy group, which has low toxicity and high solubility, and is mainly used as a solvent in various pharmaceutical and perfume industries. As a representative method for selectively synthesizing such alcohols, a Meerwein-Ponndorf-Verley (MPV) reduction reaction for reducing carbonyl compounds such as aldehydes and ketones to aluminum isopropoxide is well known. MPV reduction using aluminum requires more than equivalents of aluminum, complex complex ligands are required to use catalytic amounts, and the reaction rate is slow and the reaction must be carried out at high temperature to remove acetone from byproducts. is (Justus Liebigs Ann Chem 1925, 444 , 221;... Angew Chem 1926, 39, 138;... Bull Soc Chim Fr 1925, 37, 871;.. Synthesis 1994, 1007; Tetrahedron Lett . 1995 , 36 , 3571; Org . Lett . 2001 , 3 , 2391; Angew . Chem . Int . Ed . 2001 , 40 , 3610; Chirality 2002 , 14 , 759; Tetrahedron : Asymmetry 2005 , 16 , 3460; J. Org . Chem . 2006 , 71 , 840).

However, an example of preparing an alcohol by reducing a carbonyl compound using indium has not been reported in any literature so far, and there is a need for a method to solve the disadvantages of the MPV reduction reaction using aluminum.

In order to solve the problems of the prior art, the present invention is to replace the metal required for the MPV reduction reaction with indium to reduce the amount of use and to provide a method for producing an aldehyde derivative effectively alcohol in a short time at room temperature.

The present invention provides a method for preparing an alcohol derivative represented by the following Chemical Formula 1 through an Meerwein-Ponndorf-Verley (MPV) reduction reaction from an aldehyde derivative using indium.

[Formula 1]

Hereinafter, the present invention will be described in detail.

At this time, if there is no other definition in the technical terms and scientific terms used, it has a meaning commonly understood by those of ordinary skill in the art. Repeated descriptions of the same technical constitution and operation as those of the conventional art will be omitted.

The present invention provides a method of preparing an alcohol derivative of Formula 1 by reacting an aldehyde derivative represented by Formula 2 with an indium alkoxide derivative represented by Formula 3 below.

[Formula 1]

[Formula 2]

(3)

[In Formulas 1 to 3,

또는

이고, 상기 R의 아릴 및 헤테로아릴은 (C1-C10)알킬, (C1-C10)알콕시, 할로겐, 니트로, 시아노, (C1-C10)알킬카보닐, (C1-C10)알콕시카보닐 및 (C6-C20)아릴로 이루어진 군으로부터 선택되는 하나 이상의 치환기로 더 치환될 수 있고;R is (C1-C10) alkyl, (C3-C12) cycloalkyl, (C6-C12) aryl, (C3-C12) heteroaryl,

or

Aryl and heteroaryl of R are (C1-C10) alkyl, (C1-C10) alkoxy, halogen, nitro, cyano, (C1-C10) alkylcarbonyl, (C1-C10) alkoxycarbonyl and ( C6-C20) aryl may be further substituted with one or more substituents selected from the group consisting of;

R ¹¹ to R ¹⁵ are independently of each other hydrogen, halogen, (C 1 -C 10) alkyl or (C 3 -C 12) aryl;

R ¹ and R ² are (C 1 -C 10) alkyl.]

The "alkyl" includes both linear or pulverized carbon chains.

Specifically, in Formulas 1 and 2, R is phenyl, 2-methylphenyl, 4-methylphenyl, 2,4,6-trimethylphenyl, 2-methoxyphenyl, 3-methoxyphenyl, 4-methoxyphenyl, 3,5 Dimethoxyphenyl, 2-fluoro-4-methoxyphenyl, 4-nitrophenyl, 3-cyanophenyl, 2-iodophenyl, 2-bromophenyl, 3-bromophenyl, 4-acetylphenyl , 4-acetoxyphenyl, methoxycarbonylphenyl, 3,4- (methylenedioxy) phenyl, pyridyl, 5-bromothiophenyl, 2-phenylethenyl, 2-phenylbromoethenyl, cyclohexyl, 9-decenyl or 1,5-dimethyl-4-hexenyl.

The alcohol derivative of Formula 1 prepared by the above method is selected from compounds having the following structure, but is not limited thereto.

In the production method of the present invention, a round bottom flask or a test tube is used as the reaction vessel.

The indium alkoxide derivative of Chemical Formula 3 is preferably indium isopropoxide, and it is preferable to use 5 to 20 mol% with respect to the aldehyde derivative represented by Chemical Formula 2, using 20 mol% More preferred.

The solvent used in the preparation method of the present invention is a conventional organic solvent, toluene, dichloromethane (CH ₂ Cl ₂ ), tetrahydrofuran (THF), diethyl ether, pentane and It is preferable to use one or more selected from the group consisting of isopropanol, and more preferably to use isopropanol as a solvent.

The reaction temperature is carried out at 25 ° C to 80 ° C, more preferably at 25 ° C. The reaction time may vary depending on the reactants, the type of solvent, and the amount of the solvent. The termination of the reaction may be confirmed by TLC (Thin Layer Chromatography). After the reaction is completed, the solvent may be distilled off under reduced pressure after the extraction process, and the target product may be separated and purified through a conventional method such as column chromatography.

In the present invention, alcohol was effectively prepared using indium for the first time instead of aluminum used in the conventional Meerwein-Ponndorf-Verley (MPV) reduction reaction. In particular, unlike the conventional Meerwein-Ponndorf-Verley (MPV) reduction reaction required more than the equivalent metal and the high temperature and slow reaction rate, the present invention is a method for producing an alcohol in a high yield in a short time at room temperature. In addition, by using inexpensive and environmentally friendly isopropanol as a solvent and using indium, which is a low toxicity metal, it is a more suitable method for synthesizing alcohol derivatives used in medicine and modern industry.

Hereinafter, the configuration of the present invention will be described in more detail with reference to Examples, but the following Examples are provided to assist in understanding the present invention, and the scope of the present invention is not limited thereto.

 Example 1 Preparation of Benzyl Alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, a solvent isopropanol (1.5 mL) was added, and benzaldehyde (53 mg, 0.5 mmol) was added thereto. After stirring for 3 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound benzyl alcohol (48 mg, 88%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.37-7.34 (m, 4H), 7.32-25 (m, 1H), 4.69 (d, J = 5.9 Hz, 2H), 1.73 (d, J = 5.6 Hz, 1H)

Example 2 Preparation of 2-methylbenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, and isopropanol (1.5 mL) was added thereto, followed by o -tolualdehyde (60 mg, 0.5 mmol). After 15 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 2-methylbenzyl alcohol (57 mg, 93%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.36-7.33 (m, 1H), 7.23-16 (m, 3H), 4.69 (d, J = 3.7 Hz, 2H), 2.35 (s, 3H)

 Example 3 Preparation of 3-methylbenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and m -tolualdehyde (60 mg, 0.5 mmol) was added thereto. After 15 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain 3-methylbenzyl alcohol (53 mg, 86%) as a title compound.

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.25 (d, J = 8.0 Hz, 2H), 7.17 (d, J = 7.9 Hz, 2H), 4.64 (s, 2H), 2.35 (s, 3H)

Example 4 Preparation of 2,4,6-trimethylbenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, and isopropanol (1.5 mL) was added thereto, followed by adding mesaldehyde (74 mg, 0.5 mmol). After stirring for 4.5 hours at 80 DEG C, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain 2,4,6-trimethylbenzyl alcohol (69 mg, 92%) as a title compound.

¹ H NMR (400 MHz, CDCl ₃ ) δ 6.87 (s, 2H), 4.71 (d, J = 3.3 Hz, 2H), 2.39 (s, 6H), 2.27 (s, 3H), 1.21 (s, 1H)

Example 5 Preparation of 2-methoxybenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, a solvent isopropanol (1.5 mL) was added, and 2-methoxybenzaldehyde (68 mg, 0.5 mmol) was added thereto. After 15 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 2-methoxybenzyl alcohol (62 mg, 90%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.29 (t, J = 7.8 Hz, 2H), 6.94 (t, J = 7.4 Hz, 1H), 6.89 (d, J = 8.2 Hz, 1H), 4.69 (d , J = 5.0 Hz, 2H), 3.87 (s, 3H), 2.31 (s, 1H)

Example 6 Preparation of 4-methoxybenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, and solvent isopropanol (1.5 mL) was added, followed by 4-methoxybenzaldehyde (68 mg, 0.5 mmol). After stirring at room temperature for 5.5 hours, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 4-methoxybenzyl alcohol (54 mg, 78%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.30 (d, J = 8.6 Hz, 2H), 6.90 (td, J = 8.6, 2.4 Hz, 2H), 4.62 (s, 2H), 3.81 (s, 3H)

Example 7 Preparation of 3-methoxybenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and m -anisaldehyde (68 mg, 0.5 mmol) was added thereto. After 30 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 3-methoxybenzyl alcohol (67 mg, 97%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.29-7.25 (m, 1H), 6.94 (d, J = 7.4 Hz, 2H), 6.83 (dd, J = 7.1, 2.1 Hz, 1H), 4.67 (s, 2H), 3.82 (s, 3H)

Example 8 Preparation of 3,5-dimethoxybenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, a solvent isopropanol (1.5 mL) was added, and 3,5-dimethoxybenzaldehyde (83 mg, 0.5 mmol) was added thereto. After 30 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 3,5-dimethoxybenzyl alcohol (78 mg, 93%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 6.52 (d, J = 2.2 Hz, 2H), 6.39 (t, J = 2.3 Hz, 1H), 4.63 (s, 2H), 3.79 (s, 6H)

Example 9 Preparation of 2-fluoro-4-methoxybenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, isopropanol (1.5 mL) was added thereto, and 2-fluoro-4-methoxybenzaldehyde (77 mg, 0.5 mmol) was added thereto. After 5 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 2-fluoro-4-methoxybenzyl alcohol (76 mg, 98%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 6.99-6.94 (m, 2H), 6.79-6.75 (m, 1H), 4.73 (s, 2H), 3.79 (s, 3H)

Example 10 Preparation of 4-nitrobenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, isopropanol (1.5 mL) was added thereto, and 4-nitrobenzaldehyde (76 mg, 0.5 mmol) was added thereto. After stirring for 3 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain 4-nitrobenzyl alcohol (72 mg, 94%) as a title compound.

¹ H NMR (400 MHz, CDCl ₃ ) δ 8.23 (td, J = 8.8 Hz, 2H), 7.54 (d, J = 8.9 Hz, 2H), 4.84 (d, J = 5.5 Hz, 2H), 1.90 (t , J = 5.7 Hz, 1H)

Example 11 Preparation of 3-cyanobenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, isopropanol (1.5 mL) was added thereto, and 4-cyanobenzaldehyde (66 mg, 0.5 mmol) was added thereto. After stirring for 1 hour at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. After removing the solvent was separated by column chromatography to give the title compound 3-cyanobenzyl alcohol (60 mg, 90%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.68 (s, 1H), 7.59 (t, J = 8.6 Hz, 2H), 7.47 (t, J = 7.7 Hz, 1H), 4.75 (s, 2H), 2.07 (s, 1H)

 Example 12 Preparation of 2-iodobenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and 2-iodobenzaldehyde (116 mg, 0.5 mmol) was added thereto. After stirring for 6 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 2-iodobenzyl alcohol (110 mg, 94%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.83 (dd, J = 7.8, 1.0 Hz, 1H), 7.47 (dd, J = 7.6, 1.5 Hz, 1H), 7.37 (dt, J = 7.5, 0.9 Hz, 1H), 7.01 (dt, J = 7.6, 1.6 Hz, 1H), 4.69 (d, J = 6.1 Hz, 2H), 1.98 (t, J = 6.3 Hz, 1H)

Example 13 Preparation of 2-bromobenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and 2-bromobenzaldehyde (93 mg, 0.5 mmol) was added thereto. After 30 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 2-bromobenzyl alcohol (85 mg, 91%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.55 (dd, J = 8.0, 1.0 Hz, 1H), 7.49 (dd, J = 7.6, 1.4 Hz, 1H), 7.34 (td, J = 7.5, 1.2 Hz, 1H), 7.17 (td, J = 7.7, 1.6 Hz, 1H), 4.76 (d, J = 6.4 Hz, 2H), 2.00 (t, J = 6.5 Hz, 1H)

Example 14 Preparation of 3-bromobenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and 3-bromobenzaldehyde (93 mg, 0.5 mmol) was added thereto. After stirring for 6 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain 3-bromobenzyl alcohol (83 mg, 89%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.53 (s, 1H), 7.42 (d, J = 7.8 Hz, 1H), 7.28 (d, J = 7.6 Hz, 1H), 7.23 (t, J = 7.7 Hz , 1H), 4.68 (d, J = 5.1 Hz, 2H), 1.79 (t, J = 5.6 Hz, 1H)

Example 15 Preparation of 4-acetylbenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, and solvent isopropanol (1.5 mL) was added, followed by 4-acetylbenzaldehyde (74 mg, 0.5 mmol). After stirring at room temperature for 1.5 hours, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. After removing the solvent was separated by column chromatography to give the title compound 4-acetylbenzyl alcohol (60 mg, 80%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.92 (d, J = 8.2 Hz, 2H), 7.44 (d, J = 8.0 Hz, 2H), 4.76 (s, 2H), 2.59 (s, 3H)

Example 16 Preparation of 4-acetoxybenzyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, and solvent isopropanol (1.5 mL) was added, followed by 4-acetoxybenzaldehyde (82 mg, 0.5 mmol). After stirring for 24 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 4-acetoxybenzyl alcohol (34 mg, 41%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.38 (d, J = 8.6 Hz, 2H), 7.07 (td, J = 8.5, 2.3 Hz, 2H), 4.68 (s, 2H), 2.30 (s, 3H)

Example 17 Preparation of Methyl 4- (hydroxymethyl) benzoate

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, and solvent isopropanol (1.5 mL) was added, followed by methyl 4-formylbenzoate (82 mg, 0.5 mmol). After 30 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound methyl 4- (hydroxymethyl) benzoate (78 mg, 94%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 8.02 (d, J = 8.3 Hz, 2H), 7.43 (d, J = 8.2 Hz, 2H), 4.76 (s, 2H), 3.91 (s, 3H)

Example 18 Preparation of Piperonyl Alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, a solvent isopropanol (1.5 mL) was added, and piperonal (75 mg, 0.5 mmol) was added thereto. After stirring for 2 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound piperonyl alcohol (63 mg, 83%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 6.86 (s, 1H), 6.80 (dd, J = 8.0, 1.4 Hz, 1H), 6.77 (d, J = 7.9 Hz, 1H), 5.94 (s, 2H), 4.56 (s, 2H)

Example 19 Preparation of pyridine-3-ylmethanol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and pyridine-3-carboxaldehyde (75 mg, 0.5 mmol) was added thereto. After stirring for 1 hour at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound pyridin-3yl methanol (49 mg, 90%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 8.45 (s, 1H), 8.38 (d, J = 4.0 Hz, 1H), 7.72 (d, J = 7.9 Hz, 1H), 7.26 (q, J = 4.2 Hz , 1H), 4.68 (s, 2H)

Example 20 Preparation of (5-bromothiophen-2-yl) methanol ((5-bromothiophene-2-yl) methanol)

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and 5-bromothiophen-2-carboxaldehyde (96 mg, 0.5 mmol) was added thereto. After stirring for 1 hour at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. The mixture was extracted with ethyl acetate (10 mL x 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain (5-bromothiophen-2-yl) methanol (86 mg, 89%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 6.92 (d, J = 3.8 Hz, 1H), 6.76 (d, J = 3.5 Hz, 1H), 4.75 (s, 2H)

Example 21 Preparation of Cinnamic Alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and cinnamic aldehyde (66 mg, 0.5 mmol) was added thereto. After stirring for 5 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound cinnamil alcohol (57 mg, 85%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.40-7.38 (m, 2H), 7.34-7.29 (m, 2H), 7.26-7.22 (m, 1H), 6.62 (d, J = 15.9 Hz, 1H), 6.37 (td, J = 16.0, 5.7 Hz, 1H), 4.33 (dd, J = 5.3, 1.3 Hz, 2H)

Example 22 Preparation of α-bromocinnamyl alcohol

Indium isopropoxide (29 mg, 0.1 mmol) was added to the test tube, a solvent isopropanol (1.5 mL) was added, and α-bromosinnamaldehyde (106 mg, 0.5 mmol) was added thereto. After 30 minutes of stirring at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. After the solvent was removed, the residue was separated by column chromatography to obtain α-bromoscinnamil alcohol (102 mg, 96%) as a title compound.

¹ H NMR (400 MHz, CDCl ₃ ) δ 7.63 (d, J = 1.5 Hz, 2H), 7.39-7.35 (m, 2H), 7.34-7.32 (m, 1H), 7.09 (s, 1H), 4.42 ( d, J = 5.9 Hz, 2H)

Example 23 Preparation of Cyclohexylmethanol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and cyclohexane carboxaldehyde (56 mg, 0.5 mmol) was added thereto. After stirring for 1 hour at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound cyclohexyl methanol (52 mg, 90%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 3.44 (d, J = 6.4 Hz, 2H), 1.78-1.66 (m, 5H), 1.52-1.12 (m, 5H), 0.98-0.88 (m, 2H)

Example 24 Preparation of 10-Undeken-1-ol (10-undecen-1-ol)

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and 10-undekenal (84 mg, 0.5 mmol) was added thereto. After stirring for 3 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain 10-undeken-1-ol (70 mg, 82%) as a title compound.

¹ H NMR (400 MHz, CDCl ₃ ) δ 5.87-5.76 (m, 1H), 5.02-4.97 (m, 1H), 4.95-4.91 (m, 1H), 3.64 (q, J = 6.0 Hz, 2H), 2.07-2.01 (m, 2H), 1.58-1.53 (m, 2H), 1.39-1.29 (m, 12H), 1.23 (t, J = 4.9 Hz, 1H)

Example 25 Preparation of 2,6-dimethyl-5-heptenol

Indium isopropoxide (29 mg, 0.1 mmol) was added to a test tube, a solvent isopropanol (1.5 mL) was added, and 2,6-dimethyl-5-heptenal (84 mg, 0.5 mmol) was added thereto. After stirring for 3 hours at room temperature, 1N aqueous hydrochloric acid solution (4 mL) was added to terminate the reaction. This mixture was extracted with ethyl acetate (10 mL × 3) and washed with H ₂ O. The extracted organic layer was dried over anhydrous MgSO ₄ and filtered. The solvent was removed and the residue was separated by column chromatography to obtain the title compound 2,6-dimethyl-5-heptenol (59 mg, 83%).

¹ H NMR (400 MHz, CDCl ₃ ) δ 5.13-5.09 (m, 1H), 3.54-3.41 (m, 2H), 2.08-1.95 (m, 2H), 1.69 (s, 3H), 1.66-1.63 (m , 1H), 1.61 (s, 3H), 1.48-1.39 (m, 1H), 1.20-1.11 (m, 1H), 0.93 (d, J = 6.6 Hz, 3H)

Claims (6)

A method of preparing an alcohol derivative represented by the following Chemical Formula 1 by reacting an aldehyde derivative represented by the following Chemical Formula 2 with an indium alkoxide derivative represented by the following Chemical Formula 3.
[Formula 1]

(2)

(3)

[In Formulas 1 to 3,
R is (C1-C10) alkyl, (C3-C12) cycloalkyl, (C6-C12) aryl, (C3-C12) heteroaryl,

or

Aryl and heteroaryl of R are (C1-C10) alkyl, (C1-C10) alkoxy, halogen, nitro, cyano, (C1-C10) alkylcarbonyl, (C1-C10) alkoxycarbonyl and ( C6-C20) aryl may be further substituted with one or more substituents selected from the group consisting of;
R ¹¹ to R ¹⁵ are independently of each other hydrogen, halogen, (C 1 -C 10) alkyl or (C 3 -C 12) aryl;
R ¹ and R ² are (C 1 -C 10) alkyl.]
The method of claim 1,
R is phenyl, 2-methylphenyl, 4-methylphenyl, 2,4,6-trimethylphenyl, 2-methoxyphenyl, 3-methoxyphenyl, 4-methoxyphenyl, 3,5-dimethoxyphenyl, 2 -Fluoro-4-methoxyphenyl, 4-nitrophenyl, 3-cyanophenyl, 2-iodophenyl, 2-bromophenyl, 3-bromophenyl, 4-acetylphenyl, 4-acetoxyphenyl, Methoxycarbonylphenyl, 3,4- (methylenedioxy) phenyl, pyridyl, 5-bromothiophenyl, 2-phenylethenyl, 2-phenylbromoethenyl, cyclohexyl, 9-decenyl or 1, 5-Dimethyl-4-hexenyl.
The method of claim 1,
Indium alkoxide derivative of the formula (3) is characterized in that the indium isopropoxide (indium isopropoxide).
The method of claim 3, wherein
The indium isopropoxide is used in an amount of 5 to 20 mol% based on the aldehyde derivative of Chemical Formula 2.
The method of claim 1,
The reaction is one selected from the group consisting of toluene, dichloromethane (CH ₂ Cl ₂ ), tetrahydrofuran (THF), diethyl ether, pentane and isopropanol The production method characterized in that carried out under the above solvent.
6. The method of claim 5,
The reaction is carried out at 25 ℃ to 80 ℃ using isopropanol (isopropanol) as a solvent.