2-(2'-BROMOPHENOXY)PROPANE
2-(2'-BROMOPHENOXY)PROPANE Basic information
- Product Name:
- 2-(2'-BROMOPHENOXY)PROPANE
- Synonyms:
-
- 1-bromo-2-propan-2-yloxybenzene
- 1-Bromo-2-isopropoxybenzen
- 2-BROMOISOPROPOXYBENZENE
- 2-(2'-BROMOPHENOXY)PROPANE
- O-BROMOISOPROPOXYBENZENE
- 1-Bromo-2-isopropoxybenzene
- 1-Bromo-2-isopropoxybenzene >
- Benzene, 1-bromo-2-(1-methylethoxy)-
- CAS:
- 701-07-5
- MF:
- C9H11BrO
- MW:
- 215.09
- Product Categories:
-
- Anisoles, Alkyloxy Compounds & Phenylacetates
- Bromine Compounds
- Mol File:
- 701-07-5.mol
2-(2'-BROMOPHENOXY)PROPANE Chemical Properties
- Boiling point:
- 73 °C / 2mmHg
- Density
- 1.34
- refractive index
- 1.5360-1.5400
- storage temp.
- Sealed in dry,Room Temperature
- form
- clear liquid
- color
- Colorless to Light yellow
- Water Solubility
- Slightly soluble in water.
- CAS DataBase Reference
- 701-07-5(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- HS Code
- 2909309090
2-(2'-BROMOPHENOXY)PROPANE Usage And Synthesis
Chemical Properties
Colorless liquid
Uses
1-Bromo-2-isopropoxybenzene is used as an intermediate in organic syntheses.
Synthesis
95-56-7
75-26-3
701-07-5
General procedure for the synthesis of 1-bromo-2-isopropoxybenzene from 2-bromophenol and 2-bromopropane: A mixture of 2-bromophenol (1.156 mmol), anhydrous K2CO3 (1.20 eq., 192 mg), sodium iodide (4 mg), and anhydrous ethanol (3 mL) was magnetically stirred at room temperature under argon protection. 2-Bromopropane (1.20 eq.) was added slowly and the mixture was then refluxed for 5 hours. After the reaction was complete, it was cooled to room temperature and the solvent was removed under reduced pressure. Ethyl acetate (50 mL) was added to dissolve the residue and the organic phase was washed sequentially with 1M NaOH and brine (15 mL each). The organic phase was dried with anhydrous Na2SO4 and the solvent was evaporated under reduced pressure to obtain the crude product. Finally, the crude product was purified by fast column chromatography.
References
[1] Journal of Organic Chemistry, 2000, vol. 65, # 26, p. 9143 - 9151
[2] Journal of Medicinal Chemistry, 1998, vol. 41, # 12, p. 1997 - 2009
[3] Organic Preparations and Procedures International, 2015, vol. 47, # 3, p. 227 - 231
[4] Patent: WO2009/55674, 2009, A1. Location in patent: Page/Page column 59
[5] Journal of Medicinal Chemistry, 2012, vol. 55, # 9, p. 4189 - 4204
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