o-methylbenzyl alcohol

O-methylbenzyl alcohol structural formula

Structural formula

Business number 021M
Molecular formula C8H10O
Molecular weight 122.16
label

2-Methylbenzyl alcohol,

2-methylbenzyl alcohol,

2-Methylbenzyl alcohol,

CH3C6H4CH2OH

Numbering system

CAS number:89-95-2

MDL number:MFCD00004622

EINECS number:201-954-2

RTECS number:None

BRN number:1929783

PubChem number:24851163

Physical property data

1. Melting point (ºC): 37

2. Boiling point (ºC): 223750

3. Relative density (25℃, 4℃): 1.02340

Toxicological data

None

Ecological data

None

Molecular structure data

1. Molar refractive index: 37.52

2. Molar volume (cm3/mol): 119.5

3. Isotonic specific volume (90.2K ): 298.4

4. Surface tension (dyne/cm): 38.8

5. Polarizability (10-24cm3): 14.87

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 1

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: none

6. Topological molecule polar surface area 20.2

7. Number of heavy atoms: 9

8. Surface charge: 0

9. Complexity: 80.6

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

1. Preparation method:

O-methylbenzyldimethylethylammonium bromide (3): In a reaction bottle equipped with a stirrer and a reflux condenser, add 29.8g of o-methylbenzyldimethylamine (2) and 32.7g of bromoethane (0.3mol), 40mL of absolute ethanol, heated to reflux for 1h. Add 10.8g (0.1mol) of ethyl bromide and continue the reflux reaction for 3 hours. The ethanol and unreacted bromoethane were distilled off under reduced pressure. Add 300 mL of anhydrous ether to the remainder, filter the precipitated solid, wash the filter cake with ether, and dry under vacuum to obtain 47.5-49 g of compound (3) with a yield of 92%-95%. O-methylbenzyl acetate (4): In a reaction bottle equipped with a stirrer, add 38.7g (0.15mol) of compound (3), 24.6g (0.3mol) of molten sodium acetate, and 100mL of glacial acetic acid, and heat to reflux for 24 hours. . Cool to room temperature, pour 250 mL of water, and neutralize with 84 g of sodium bicarbonate. Extract with ether three times, combine the ether layers, wash with saturated sodium bicarbonate solution and saturated brine in sequence, and dry over anhydrous magnesium sulfate. Recover ether and then distill under reduced pressure to collect 119~121℃/2.0kPa or 129~131℃/2.8kPaFraction, 21.6~22.4g of o-methylbenzyl acetate (4) was obtained, with a yield of 88%~91%. O-methylbenzyl alcohol (1): Add 50 mL of water, 5 g of sodium hydroxide (0.12 mol), 16.4 g (0.1 mol) of the above compound (4), and 50 mL of methanol into the reaction bottle, and heat to reflux for 2 hours. After cooling, add 50 mL of water and extract with ether three times. The ether layers were combined, washed with water, washed with saturated brine, and dried over anhydrous sodium sulfate. After recovering the ether, add 50 mL of petroleum ether and freeze in an ice-salt bath. The precipitated solid was suction-filtered, washed with cold petroleum ether, and dried to obtain 11.6 to 11.8 g of o-methylbenzyl alcohol (1), with a yield of 95% to 97%. [1]

Purpose

None

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/28806

author:

Previous article
Next article
Contact Us

Contact us

+86 - 152 2121 6908

Online consultation: QQ交谈

E-mail: sales@newtopchem.com

Working hours: Monday to Friday, 9:00-17:30, closed on holidays
Follow wechat
Scan wechat and follow us

Scan wechat and follow us

Follow Weibo
Back to top
Home
E-mail
Products
Search