5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE

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5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE manufacturers

5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE Basic information
Product Name:5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE
Synonyms:5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE;5-hydroxy-2,2-dimethylchromene-6-carbaldehyde;2H-1-Benzopyran-6-carboxaldehyde, 5-hydroxy-2,2-dimethyl-
CAS:54287-99-9
MF:C12H12O3
MW:204.22
EINECS:
Product Categories:
Mol File:54287-99-9.mol
5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE Structure
5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE Chemical Properties
Melting point 70-71 °C(Solv: heptane (142-82-5))
Boiling point 310.0±42.0 °C(Predicted)
density 1+-.0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka7.76±0.40(Predicted)
AppearanceOff-white to light yellow Solid
Safety Information
MSDS Information
5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE Usage And Synthesis
Synthesis
3-Methyl-2-butenal

107-86-8

2,4-Dihydroxybenzaldehyde

95-01-2

5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE

54287-99-9

The general procedure for the synthesis of 5-hydroxy-2,2-dimethyl-2H-chromene-6-carbaldehyde from 3-methyl-2-butenal and 2,4-dihydroxybenzaldehyde was as follows: 2,4-dihydroxybenzaldehyde (15) (3 g, 20.17 mmol), calcium hydroxide (1.543 g, 20.8 mmol), and 150 mL of methanol were added to a two-necked round-bottom flask. Subsequently, 3-methyl-2-butenal (9.135 g, 108.6 mmol) was added slowly and dropwise. The reaction mixture was stirred continuously at room temperature for 48 hours. After completion of the reaction, the pH of the reaction solution was adjusted to 1-2 with 1 M hydrochloric acid to quench the reaction. Methanol was removed by distillation under reduced pressure and the remaining aqueous phase was extracted with ethyl acetate (3 x 150 mL). The organic phases were combined, washed sequentially with brine (2 × 100 mL), dried over anhydrous sodium sulfate, filtered and the organic solvent was concentrated under reduced pressure. The crude product was purified by silica gel fast column chromatography (eluent: hexane/ethyl acetate, 9:1). The final product 5-hydroxy-2,2-dimethyl-2H-chromene-6-carboxaldehyde (16) was crystallized using a solvent mixture of hexane/ethyl acetate (3:1) to give a yellow solid (2.06 g, 50% yield).

References[1] Journal of Medicinal Chemistry, 2018,
[2] Journal of Organic Chemistry, 2015, vol. 80, # 22, p. 11460 - 11467
[3] Angewandte Chemie - International Edition, 2012, vol. 51, # 32, p. 8092 - 8096
[4] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 11, p. 2941 - 2959
[5] European Journal of Medicinal Chemistry, 2013, vol. 69, p. 798 - 816
5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE Preparation Products And Raw materials
Raw materials3-Methyl-2-butenal-->3-Methyl butynol-->2-Methyl-2-butene-->2,4-Dihydroxybenzaldehyde-->Calcium hydroxide-->Methanol
Tag:5-HYDROXY-2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE(54287-99-9) Related Product Information
5-HYDROXYDEQUELIN GAMBOGIC ACID calophyllolid DEGUELIN ISO-OSAJIN MACLURAXANTHONE OSAJIN 2-Butenal, 2-methyl-4-[3a,4,5,7-tetrahydro-8-hydroxy-3,3,11,11-tetramethyl-13-(3-methyl-2-butenyl)-7,15-dioxo-1,5-methano-1H,3H,11H-furo[3,4-g]pyrano[3,2-b]xanthen-1-yl]-, [1R-[1alpha,1(Z),3abeta,5alpha,14aS*]]- (-)-TEPHROSIN ISOPOMIFERIN ISOPOMIFERIN-3',4'-DIMETHYL ETHER 5-METHOXYDURMILLONE Pongapinone A POMIFERIN-3',4'-DIMETHYL ETHER MILLETTONE ISO-OSAJIN-4'-METHYL ETHER 6A,12A-DEHYDROMILLETONE ICHTHYNONE