2-CHLORO-3-METHOXYBENZALDEHYDE

2-CHLORO-3-METHOXYBENZALDEHYDE Property

Melting point:

53-58 °C (lit.)

Boiling point:

260℃

Density 

1.244

Flash point:

115℃

storage temp. 

2-8°C, stored under nitrogen

form 

powder to crystal

color 

White to Light yellow to Green

Safety

Hazard Codes 

Xn,N

Risk Statements 

22-36/37/38-50

Safety Statements 

26-36-45-60-61

RIDADR 

UN 3077 9/PG 3

WGK Germany 

2

HazardClass 

9

PackingGroup 

III

HS Code 

2914500090

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

H400Very toxic to aquatic life

Precautionary statements

P273Avoid release to the environment.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

2-CHLORO-3-METHOXYBENZALDEHYDE Chemical Properties,Usage,Production

Uses

2-Chloro-3-methoxybenzaldehyde is an organic compound mainly used in the field of organic synthesis and can be used as a raw material for dyes, coatings and fragrances.

Synthesis

1. tBuOCl (20 mL, 176 mmol) is slowly added to a suspension of 3-hydroxybenzaldehyde (20.12 g, 160 mmol) in acetic acid (40 mL) under stirring conditions. The reaction solution became clarified and significantly exothermic. The reaction mixture was cooled and stirred continuously for 16 hours to produce a white precipitate. The solid product was collected by filtration, washed with water and dried to give 2-chloro-3-hydroxybenzaldehyde (13.77 g, 55% yield). gCMS (EI) m/z 156, 158 (M+). 2. 2-Chloro-3-hydroxybenzaldehyde (4.55 g, 29 mmol) was dissolved in DMF (30 mL), K2CO3 (4.8 g, 34.9 mmol) was added followed by iodomethane (2.7 mL, 43.6 mmol). The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the solvent was removed by concentration under reduced pressure, and the residue was dissolved in ethyl acetate, washed sequentially with water and brine, dried over Na2SO4 and concentrated. Purification by silica gel column chromatography using ethyl acetate/hexane (1:5) as eluent afforded 2-chloro-3-methoxybenzaldehyde (4.68 g, 94% yield) as a colorless oil, which solidified on standing. gCMS (EI) m/z 170, 172 (M+).

References

[1] Organic Letters, 2018, vol. 20, # 5, p. 1388 - 1391
[2] Patent: WO2017/127371, 2017, A1. Location in patent: Page/Page column 17
[3] Patent: WO2005/7164, 2005, A1. Location in patent: Page 30-31
[4] Patent: WO2005/7165, 2005, A1. Location in patent: Page 46
[5] Patent: WO2005/7633, 2005, A1. Location in patent: Page 33