2,3-DIHYDRO-1-BENZOFURAN-7-CARBALDEHYDE
2,3-DIHYDRO-1-BENZOFURAN-7-CARBALDEHYDE Basic information
- Product Name:
- 2,3-DIHYDRO-1-BENZOFURAN-7-CARBALDEHYDE
- Synonyms:
-
- 2,3-Dihydro-1-benzofurane-7-carbaldehyde
- 7-Benzofurancarboxaldehyde, 2,3-dihydro- (9CI)
- 2,3-Dihydrobenzo[b]furan-7-aldehyde
- 2,3-Dihydro-1-benzofuran-7-carboxaldehyde, 2,3-Dihydro-7-formyl-1-benzofuran
- 2,3-Dihydrobenzo[b]furan-7-carboxaldehyde
- BUTTPARK 97\04-63
- 2,3-DIHYDRO-1-BENZOFURAN-7-CARBALDEHYDE
- 2,3-DIHYDROBENZOFURAN-7-CARBOXALDEHYDE
- CAS:
- 196799-45-8
- MF:
- C9H8O2
- MW:
- 148.16
- Product Categories:
-
- ALDEHYDE
- Mol File:
- 196799-45-8.mol
2,3-DIHYDRO-1-BENZOFURAN-7-CARBALDEHYDE Chemical Properties
- Melting point:
- 53-54 °C
- Boiling point:
- 277.6±29.0 °C(Predicted)
- Density
- 1.222±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- White to yellow Solid
- CAS DataBase Reference
- 196799-45-8
Safety Information
- Risk Statements
- 52
- HS Code
- 2932990090
2,3-DIHYDRO-1-BENZOFURAN-7-CARBALDEHYDE Usage And Synthesis
Synthesis
151155-53-2
196799-45-8
The general procedure for the synthesis of 2,3-dihydrobenzofuran-7-carbaldehyde using 2,3-dihydrobenzofuran-7-methanol as starting material was as follows: 2,3-dihydrobenzofuran-7-methanol (9.76 g, 64.99 mmol) was mixed with manganese dioxide (45.2 g, 519.93 mmol) in toluene (250 mL), and the reaction was stirred for 3 hours at 60 °C. Upon completion of the reaction, manganese dioxide was removed by filtration and the filtrate was concentrated under reduced pressure. Subsequently, the precipitate precipitated was collected by filtration and washed with cooled hexane to give 2,3-dihydrobenzofuran-7-carbaldehyde (7.43 g, 50.1 mmol, 77% yield) as a light yellow solid.
References
[1] Patent: TW2016/2105, 2016, A. Location in patent: Paragraph 1203
[2] Patent: WO2007/25307, 2007, A2. Location in patent: Page/Page column 305 - 306
[3] Patent: WO2008/106139, 2008, A1. Location in patent: Page/Page column 475
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