Basic information Safety Supplier Related

2,3-Dihydrobenzo[b]furan-5-carbaldehyde

Basic information Safety Supplier Related

2,3-Dihydrobenzo[b]furan-5-carbaldehyde Basic information

Product Name:
2,3-Dihydrobenzo[b]furan-5-carbaldehyde
Synonyms:
  • AKOS MSC-0772
  • 5-Benzofurancarboxaldehyde, 2,3-dihydro- (6CI,9CI)
  • 2,3-Dihydro-5-benzofurancarbox
  • 2,3-dihyro-1-benzofuran-5-carb
  • 2,3-Dihydrobenzo[b]furan-5-carbaldehyde, 95+%
  • 2,3-DIBENZO[B]FURAN-5-CARBOXALDEHYDE
  • 2,3-DIHYDRO-1-BENZOFURAN-5-CARBALDEHYDE
  • 2,3-DIHYDROBENZOFURAN-5-CARBALDEHYDE
CAS:
55745-70-5
MF:
C9H8O2
MW:
148.16
EINECS:
259-788-1
Product Categories:
  • Heterocycle intermediates
  • Pharmaceutical intermediate
  • Benzofurans
  • Building Blocks
  • Heterocyclic Building Blocks
  • Aromatics
  • Aromatics Compounds
  • Furans
  • ALDEHYDE
  • Fluorobenzene
  • Carbonyl Compounds
  • Heterocycles
Mol File:
55745-70-5.mol
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2,3-Dihydrobenzo[b]furan-5-carbaldehyde Chemical Properties

Melting point:
191~193℃
Boiling point:
88-89 °C/0.1 mmHg (lit.)
Density 
1.177 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.6000(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C(protect from light)
form 
clear liquid
color 
Colorless to Light orange to Yellow
CAS DataBase Reference
55745-70-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
43
Safety Statements 
37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29329990

MSDS

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2,3-Dihydrobenzo[b]furan-5-carbaldehyde Usage And Synthesis

Chemical Properties

White to light yellow liquid

Uses

Hair dye composition.

Synthesis

496-16-2

68-12-2

55745-70-5

2,3-Dihydrobenzofuran-5-carbaldehyde was synthesized as follows: in a dry reaction flask, 2,3-dihydrobenzofuran (100 g, 0.833 mol) was dissolved in N,N-dimethylformamide (355.0 ml). Under stirring, phosphorus oxychloride (255.58 g, 1.666 mol) was slowly added dropwise, and the reaction temperature was controlled to be maintained between 80°C and 85°C. The reaction mixture was stirred continuously at this temperature for 4 to 5 hours, during which the progress of the reaction was monitored by high performance liquid chromatography (HPLC). Upon completion of the reaction, the mixture was carefully poured into ice water to quench the reaction. Subsequently, the organic layer was separated by extraction with toluene (2000 ml). The organic layer was washed sequentially with 5% sodium bicarbonate solution (500 ml) and 10% brine solution (500 ml) to remove residual acid and DMF.The washed organic layer was subjected to distillation under reduced pressure at 50 °C to 60 °C to remove the solvent to give the crude product. By further purification, 2,3-dihydrobenzofuran-5-carbaldehyde was obtained in 85% to 90% yield and 90% to 92% purity.

References

[1] Patent: EP1792899, 2007, A1. Location in patent: Page/Page column 11
[2] Patent: WO2010/41271, 2010, A2. Location in patent: Page/Page column 28
[3] Letters in Drug Design and Discovery, 2013, vol. 10, # 7, p. 561 - 571
[4] Patent: CN102766135, 2017, B. Location in patent: Paragraph 0035-0036
[5] Journal of Medicinal Chemistry, 2002, vol. 45, # 19, p. 4222 - 4239

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