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2-CHLORO-3-METHOXYBENZALDEHYDE

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2-CHLORO-3-METHOXYBENZALDEHYDE Basic information

Product Name:
2-CHLORO-3-METHOXYBENZALDEHYDE
Synonyms:
  • 2-CHLORO-3-METHOXYBENZALDEHYDE,98.0+%(GC)
  • 2-Chloro-3-methoxybenzaldehyde 97%
  • 2-Chloro-m-anisaldehyde
  • 2-Chloro-3-methoxybenzaldehyde >
  • Benzaldehyde, 2-chloro-3-methoxy-
  • (2E)-3-(5-methyl-37-furyl)acrylic acid
CAS:
54881-49-1
MF:
C8H7ClO2
MW:
170.59
Product Categories:
  • Aldehydes
  • C8
  • Carbonyl Compounds
Mol File:
54881-49-1.mol
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2-CHLORO-3-METHOXYBENZALDEHYDE Chemical Properties

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
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Safety Information

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
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2-CHLORO-3-METHOXYBENZALDEHYDE Usage And Synthesis

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

56962-10-8

74-88-4

54881-49-1

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

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