4-TERT-BUTYL-2,6-DIFORMYLPHENOL
4-TERT-BUTYL-2,6-DIFORMYLPHENOL Basic information
- Product Name:
- 4-TERT-BUTYL-2,6-DIFORMYLPHENOL
- Synonyms:
-
- 5-(tert-Butyl)-2-hydroxybenzene-1,3-dicarboxaldehyde, 4-(tert-Butyl)-2,6-diformylphenol
- 5-(TERT-BUTYL)-2-HYDROXYISOPHTHALALDEHYDE
- AKOS BC-1732
- 4-TERT-BUTYL-2,6-DIFORMYLPHENOL
- 5-(1,1-DIMETHYLETHYL)-2-HYDROXY-1,3-BENZENEDICARBOXALDEHYDE
- 4-tert-Butyl-2,6-diforMylphenol 96%
- 4-tert-Butyl-2,6-diformylphenol,5-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedicarboxaldehyde
- 4-tert-Butyl-2,6-diformylphenol
- CAS:
- 84501-28-0
- MF:
- C12H14O3
- MW:
- 206.24
- Product Categories:
-
- Aldehydes
- Building Blocks
- C10-C12
- Carbonyl Compounds
- Chemical Synthesis
- Organic Building Blocks
- Mol File:
- 84501-28-0.mol
4-TERT-BUTYL-2,6-DIFORMYLPHENOL Chemical Properties
- Melting point:
- 99-103 °C(lit.)
- Boiling point:
- 267.8±40.0 °C(Predicted)
- Density
- 1.159±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- powder
- pka
- 6.61±0.23(Predicted)
- color
- yellow
MSDS
- Language:English Provider:SigmaAldrich
4-TERT-BUTYL-2,6-DIFORMYLPHENOL Usage And Synthesis
Uses
1. Used as a key intermediate for the production of a BODIPY chemodosimetric sensor for cyanide ions. 2. Used as a key intermediate for a Pro-ligand in bimetallic catalysis.
General Description
4-tert-Butyl-2,6-diformylphenol can be prepared from 4-tert-butylphenol and hexamethylenetetramine.
Synthesis
2203-14-7
84501-28-0
The general procedure for the synthesis of 4-tert-butyl-2,6-formylphenol from (5-(tert-butyl)-2-hydroxy-1,3-phenyl)dimethanol was as follows: activated MnO2 (40 g) was added to CHCl3 (200 mL) in a 500 mL round-bottom flask. The mixture was heated under stirring to reflux for about 15 minutes, then powder of (5-(tert-butyl)-2-hydroxy-1,3-phenyl)dimethanol (5.0 g) was added slowly. After keeping the reaction at reflux for 8 hours, the reaction mixture was cooled to room temperature and filtered through a Brinell funnel. The solid residue was washed thoroughly with CHCl3 (40 mL x 5) until the filtrate was colorless. The filtrates were combined and concentrated using a rotary evaporator to give the yellow solid product 4-tert-butyl-2,6-formylphenol (3.8 g, 77% yield).
References
[1] Synthetic Communications, 2000, vol. 30, # 9, p. 1555 - 1561
[2] Tetrahedron Letters, 2012, vol. 53, # 7, p. 804 - 807
[3] Bulletin of the Chemical Society of Japan, 1984, vol. 57, # 9, p. 2683 - 2684
[4] Chemische Berichte, 1994, vol. 127, # 3, p. 465 - 476
[5] Chemische Berichte, 1942, vol. 75, p. 363,366
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