(2-Bromoethyl)benzene

(2-Bromoethyl)benzene
  • CAS No.:103-63-9

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  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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(2-Bromoethyl)benzene Basic information
Product Name:(2-Bromoethyl)benzene
Synonyms:1-BROMO-2-PHENYLETHANE;PHENYL ETHYL BROMIDE;PHENETHYL BROMIDE;(2-bromoethyl)-benzen;.beta.-Phenylethylbromide;2-Phenethyl bromide;2-phenethylbromide;2-Phenyl-1-bromoethane
CAS:103-63-9
MF:C8H9Br
MW:185.06
EINECS:203-130-8
Product Categories:fine chemicals;103-63-9
Mol File:103-63-9.mol
(2-Bromoethyl)benzene Chemical Properties
Melting point -56 °C
Boiling point 220-221 °C(lit.)
density 1.355 g/mL at 25 °C(lit.)
refractive index n20/D 1.556(lit.)
Fp 193 °F
storage temp. 2-8°C
solubility 0.039g/l
form Liquid
color Clear colorless to pale yellow
Water Solubility INSOLUBLE
BRN 507487
Stability:Stable. Incompatible with strong oxidizing agents.
InChIKeyWMPPDTMATNBGJN-UHFFFAOYSA-N
CAS DataBase Reference103-63-9(CAS DataBase Reference)
NIST Chemistry Reference1-Bromo-2-phenylethane(103-63-9)
EPA Substance Registry SystemBenzene, (2-bromoethyl)- (103-63-9)
Safety Information
Hazard Codes Xn
Risk Statements 22-36-36/37/38
Safety Statements 26-37/39-39
RIDADR UN 1993 / PGIII
WGK Germany 3
RTECS CY9032000
TSCA Yes
HS Code 29036990
Hazardous Substances Data103-63-9(Hazardous Substances Data)
MSDS Information
ProviderLanguage
1-Bromo-2-phenylethane English
SigmaAldrich English
ACROS English
ALFA English
(2-Bromoethyl)benzene Usage And Synthesis
DescriptionPhenethylbromide is an analytical reference material that is structurally categorized as an organobromide. It is used in the synthesis of a variety of compounds, including fentanyl. Phenethylbromide is combined with 4-piperidinone to produce N-phenethyl-4-piperidone, which, as a precursor in the synthesis of fentanyl (Item Nos. ISO60197 | 14719), is scheduled as a List I chemical in the United States. Phenethylbromide may be found as in impurity in samples of fentanyl produced using this pathway.
Chemical Propertiescolourless to yellow liquid. It is miscible with ether and benzene, but insoluble in water.
Uses(2-Bromoethyl)benzene is used in the preparation of phenelzine by reacting with hydrazine. It is also used as a starting material to prepare various beta-phenethyl derivatives, active pharmaceutical ingredients, and fragrances. It finds application as a flame retardant.
Preparation(2-Bromoethyl)benzene is synthesized by the reaction of phenethyl alcohol with hydrogen bromide.Reaction: The phenethyl alcohol was heated to 110°C, hydrogen bromide was slowly introduced, and the reaction was refluxed. The reaction was completed, cooled, washed with water, 10% sodium carbonate solution, and water in turn. After drying with anhydrous potassium carbonate, fractional distillation under reduced pressure was carried out to collect fractions at 97-99°C (2.0 kPa) with a yield of over 90%.
Synthesis Reference(s)The Journal of Organic Chemistry, 29, p. 2317, 1964 DOI: 10.1021/jo01031a051Synthetic Communications, 20, p. 2349, 1990 DOI: 10.1080/00397919008053179
SynthesisPhenethylbromide is usually manufactured by the free-radical addition of HBr to styrene.The typical batch process is run in a glasslined reactor by sparging gaseous HBr through a solution of styrene in an inert solvent containing a free-radical initiator. The reaction, which is rapid and moderately exothermic, can be controlled by introducing HBr at about the rate it is consumed. When styrene is completely converted, any excess HBr that is present can be recovered by various techniques prior to recovery of solvent and product by distillation.
Purification MethodsWash the bromide with conc H2SO4, water, aqueous 10% Na2CO3 and water again, then dry it with CaCl2 and fractionally distil it just before use. [Beilstein 5 IV 907.]

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