| Identification | Back Directory | [Name]
5-TERT-BUTYL-2-HYDROXY-BENZALDEHYDE | [CAS]
2725-53-3 | [Synonyms]
5-TERT-BUTYLSALICYLALDEHYDE
5-t-Butyl-2-hydroxybenzaldehyde
2-Hydroxy-5-tert-butylbenzaldehyde
5-TERT-BUTYL-2-HYDROXY-BENZALDEHYDE
5-tert-Butyl-2-hydroxybenzaldehyde 98%
5-tert-Butyl-2-hydroxybenzaldehyde, >=95%
5-(TERT-BUTYL)-2-HYDROXYBENZENECARBALDEHYDE
Benzaldehyde,5-(1,1-diMethylethyl)-2-hydroxy-
5-tert-Butyl-2-hydroxybenzaldehyde,5-tert-Butylsalicylaldehyde | [Molecular Formula]
C11H14O2 | [MDL Number]
MFCD01321335 | [MOL File]
2725-53-3.mol | [Molecular Weight]
178.23 |
| Chemical Properties | Back Directory | [Melting point ]
100-103 °C | [Boiling point ]
251-252 °C/729 mmHg (lit.) | [density ]
1.039 g/mL at 25 °C (lit.) | [refractive index ]
n20/D 1.539(lit.)
| [Fp ]
220 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [pka]
8.39±0.18(Predicted) | [Appearance]
Colorless to light yellow Liquid | [InChI]
InChI=1S/C11H14O2/c1-11(2,3)9-4-5-10(13)8(6-9)7-12/h4-7,13H,1-3H3 | [InChIKey]
ZVCQQLGWGRTXGC-UHFFFAOYSA-N | [SMILES]
C(=O)C1=CC(C(C)(C)C)=CC=C1O |
| Hazard Information | Back Directory | [Uses]
5-tert-Butyl-2-hydroxybenzaldehyde is a general chemical reactant/reagent used in the synthesis of Vanadium (V) amino phenolato antitumor agents. As well, its used in the synthesis of dibutyltin complexes for their cytotoxic activity. | [Synthesis]
Hexamethylenetetramine (4.77 g, 34.0 mmol) and 4-tert-butylphenol (2.55 g, 17.0 mmol) were dissolved in anhydrous trifluoroacetic acid (30 mL) under nitrogen atmosphere. The reaction mixture was heated to 80 °C and refluxed for 24 hours. Upon completion of the reaction, the mixture was slowly poured into 4 M hydrochloric acid solution (100 mL) and stirred for 10 min, followed by extraction with dichloromethane (2 x 100 mL). The organic phases were combined and washed sequentially with 4 M hydrochloric acid solution (2 × 100 mL) and deionized water (100 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography with dichloromethane as eluent to obtain the target product 5-tert-butyl-2-hydroxybenzaldehyde (1.85 g, yield 61.06%) in the form of yellow viscous liquid. | [References]
[1] Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2018, vol. 204, p. 657 - 664
[2] Synthesis, 1998, # 7, p. 1029 - 1032
[3] Monatshefte fuer Chemie, 1950, vol. 81, p. 1098,1106
[4] Journal of the American Chemical Society, 1950, vol. 72, p. 4324 |
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