METHYL ALPHA-BROMOPHENYL ACETATE
- Product Name
- METHYL ALPHA-BROMOPHENYL ACETATE
- CAS No.
- 704-65-4
- Chemical Name
- METHYL ALPHA-BROMOPHENYL ACETATE
- Synonyms
- 2-Acetoxybenzyl bromide;2-(Bromomethyl)phenyl acetate;2-Acetoxyphenylmethyl bromide;Phenol, 2-(bromomethyl)-, 1-acetate
- CBNumber
- CB2506566
- Molecular Formula
- C9H9BrO2
- Formula Weight
- 229.07
- MOL File
- 704-65-4.mol
METHYL ALPHA-BROMOPHENYL ACETATE Property
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- form
- fused solid
- color
- White
Safety
- HS Code
- 2915390090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H319Causes serious eye irritation
- Precautionary statements
-
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- B847225
- Product name
- 2-(Bromomethyl)phenylAcetate
- Packaging
- 100mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- OR400175
- Product name
- 2-(Bromomethyl)phenylacetate
- Packaging
- 500mg
- Price
- $203
- Updated
- 2021/12/16
- Product number
- OR400175
- Product name
- 2-(Bromomethyl)phenylacetate
- Packaging
- 1g
- Price
- $319
- Updated
- 2021/12/16
- Product number
- 2723-9-18
- Product name
- 2-(Bromomethyl)phenyl acetate
- Packaging
- 1g
- Price
- $352
- Updated
- 2021/12/16
- Product number
- 2723-9-18
- Product name
- 2-(Bromomethyl)phenyl acetate
- Packaging
- 500mg
- Price
- $224
- Updated
- 2021/12/16
METHYL ALPHA-BROMOPHENYL ACETATE Chemical Properties,Usage,Production
Synthesis
533-18-6
704-65-4
General method: o-tolyl acetate (3.18 g, 15 mmol) and N-bromosuccinimide (2.67 g, 15 mmol) were dissolved in dry carbon tetrachloride (60 ml), and the reaction mixture was stirred for 1 hr under the irradiation of 150 W tungsten lamp. After completion of the reaction, the mixture was cooled to room temperature and the precipitated succinimide was removed by filtration. The filtrate was concentrated under reduced pressure to remove the solvent and the resulting crude product was purified by silica gel column chromatography using a solvent mixture of ethyl acetate with petroleum ether (60-80 °C boiling range, 10% v/v) as eluent to give phenyl 2-(bromomethyl)acetate (3a). It was further recrystallized from a mixed solvent of ethyl ether and petroleum ether (60-80 °C boiling range) to obtain colorless shiny granular crystals.
References
[1] Organic Letters, 2009, vol. 11, # 16, p. 3670 - 3673
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1993, # 12, p. 1359 - 1366
[3] Tetrahedron Letters, 2011, vol. 52, # 18, p. 2423 - 2423
[4] Inorganic Chemistry, 2017, vol. 56, # 1, p. 470 - 479
[5] Acta Chemica Scandinavica, 1997, vol. 51, # 12, p. 1162 - 1168
METHYL ALPHA-BROMOPHENYL ACETATE Preparation Products And Raw materials
Raw materials
Preparation Products
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