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2-(4-BROMOPHENYL)PROPAN-2-OL

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CAS:2077-19-2
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CAS:2077-19-2
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CAS:2077-19-2
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CAS:2077-19-2

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  • $101.00 / 1KG
  • 2025-09-25
  • CAS:2077-19-2
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  • Purity: 99%
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2-(4-BROMOPHENYL)PROPAN-2-OL Basic information
Product Name:2-(4-BROMOPHENYL)PROPAN-2-OL
Synonyms:2-(4-BROMOPHENYL)PROPAN-2-OL;4-Bromophenyldimethylcarbinol;p-Bromo-alpha,alpha-dimethylbenzyl alcohol;p-Bromocumyl alcohol;2-(4-BroMophenyl)-2-propanol;Benzenemethanol, 4-bromo-α,α-dimethyl-;2-(4-Bromophenyl)-2-propanol,98%;4-Bromo-alpha,alpha-dimethylbenzyl Alcohol
CAS:2077-19-2
MF:C9H11BrO
MW:215.09
EINECS:
Product Categories:
Mol File:2077-19-2.mol
2-(4-BROMOPHENYL)PROPAN-2-OL Structure
2-(4-BROMOPHENYL)PROPAN-2-OL Chemical Properties
Melting point 45.6℃
Boiling point 75-85℃ /0.1mm
density 1.356
refractive index 1.5520
storage temp. Sealed in dry,Room Temperature
pka14.29±0.29(Predicted)
form Solid
color White
Water Solubility Slightly soluble in water (1.4 g/L) (25°C)
Safety Information
HS Code 2905599890
MSDS Information
2-(4-BROMOPHENYL)PROPAN-2-OL Usage And Synthesis
UsesIt is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. It is a medicine intermediate.
Synthesis
Methylmagnesium Bromide

75-16-1

4'-Bromoacetophenone

99-90-1

2-(4-BROMOPHENYL)PROPAN-2-OL

2077-19-2

1. 1-(4-Bromophenyl)ethanone (9.25 g, 46.5 mmol) was dissolved in tetrahydrofuran (200 mL). 2. The reaction system was cooled at -50 °C in a low temperature bath. 3. An ether solution of methylmagnesium bromide (3 M, 46.5 mL, 139 mmol) was added slowly and dropwise over 15 minutes. 4. After the dropwise addition, the reaction system was allowed to warm gradually to room temperature and stirring was continued for 20 hours. 5. Upon completion of the reaction, the reaction was quenched with saturated aqueous ammonium chloride solution. 6. The reaction mixture was extracted with ethyl acetate and the organic phases were combined. 7. The organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to obtain the crude product as an oil. 8. The crude product was purified by silica gel column chromatography (eluent: 0-20% ethyl acetate/hexane gradient elution) to afford the target product 2-hydroxy-2-(4-bromophenyl)propane (9.1 g, 46.2 mmol, 91% yield). 9. The product was identified by mass spectrometry (MS). 9. The product was characterized by mass spectrometry (ESI): m/z 197.1 [M] , 199.1 [M+2]

References[1] Journal of Medicinal Chemistry, 1995, vol. 38, # 17, p. 3368 - 3383
[2] Patent: WO2010/62571, 2010, A1. Location in patent: Page/Page column 92
[3] Journal of the Chemical Society - Perkin Transactions 1, 1997, # 15, p. 2169 - 2174
[4] Journal of the American Chemical Society, 1971, vol. 93, p. 6877 - 6887
[5] Journal of the American Chemical Society, 1999, vol. 121, # 14, p. 3557 - 3558
2-(4-BROMOPHENYL)PROPAN-2-OL Preparation Products And Raw materials
Raw materials1,4-Dibromobenzene-->Ethyl 4-bromobenzoate-->Methyl 4-bromobenzoate-->Methylmagnesium Bromide-->Acetone-->4'-Bromoacetophenone-->Tetrahydrofuran-->Diethyl ether-->Ammonium chloride
Tag:2-(4-BROMOPHENYL)PROPAN-2-OL(2077-19-2) Related Product Information
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