Phenethylboronic acid Chemical Properties

Melting point:

76-81 °C (lit.)

Boiling point:

310.4±35.0 °C(Predicted)

Density 

1.077±0.06 g/cm3(Predicted)

storage temp. 

Inert atmosphere,Store in freezer, under -20°C

form 

powder to crystal

pka

10.12±0.43(Predicted)

color 

White to Almost white

InChI

InChI=1S/C8H11BO2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5,10-11H,6-7H2

InChIKey

VPRUMANMDWQMNF-UHFFFAOYSA-N

SMILES

B(CCC1=CC=CC=C1)(O)O

CAS DataBase Reference

34420-17-2(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

26-36

WGK Germany 

3

HazardClass 

IRRITANT

HS Code 

2931900090

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Phenethylboronic acid Usage And Synthesis

Chemical Properties

off-white powder

Uses

Phenethylboronic acid is a good inhibitor of chymotrypsin.

Uses

2-Phenylethylboronic acid is used as a reactant in Suzuki-Miyaura cross-coupling reactions, reactions with α-diazocarbonyl compounds, C-H functionalization of quinones, cross-coupling with aromatic amines and arylation & alkylation of diphenylisoxazole. It has been also used as reactant in studies of the stability of boronic esters to hydrolysis.

Uses

Reactant involved in:• ;Suzuki-Miyaura cross-coupling reactions1• ;Reactions with α-diazocarbonyl compounds2• ;C-H functionalization of quinones3• ;Cross-coupling with aromatic amines4• ;Arylation and alkylation of diphenylisoxazole5Reactant used in studies of the stability of boronic esters to hydrolysis6

Synthesis

A solution was prepared by dissolving styrene (2.083 g, 20 mmol) and trimethylsilane (1.484 g, 20 mmol) in hexane (6 mL) at -80 °C. The solution was slowly added dropwise to a solution of BBr3 (5.010 g, 20 mmol) in hexane (6 mL). The reaction system was controlled to gradually warm up to room temperature over a period of 2 hours. Upon completion of the reaction, the solvent was removed by evaporation under vacuum. Water (4 mL) was added to the residue, at which point the release of gaseous HBr and an increase in the temperature of the system was observed. After cooling the system to room temperature, the solvent was again evaporated under vacuum. The resulting white precipitate was purified by recrystallization from a minimal amount of water to give 2.73 g (69% yield) of 2-phenylethylboronic acid. Methanol (0.81 mL, 20 mmol) was added to a suspension of 2-phenylethylboronic acid (1.5 g, 10 mmol) in pentane (6 mL) and the reaction was stirred for 20 min at room temperature. MgSO4 was then added and stirring was continued for 10 minutes before the organic phase was separated. Methanol (0.81 mL, 20 mmol) was added again to the aqueous phase and stirred at room temperature for 20 min before adding MgSO4 and stirring for 10 min to separate the organic phase. All organic phase extracts were combined, concentrated and the residue was purified by vacuum distillation to give 1.19 g (67% yield) of a colorless liquid dimethyl 2-phenylborate.

References

[1] Tetrahedron Letters, 2003, vol. 44, # 42, p. 7789 - 7792
[2] Tetrahedron Letters, 2011, vol. 52, # 41, p. 5259 - 5263
[3] Journal of Organic Chemistry, 2008, vol. 73, # 5, p. 1898 - 1905
[4] Patent: WO2008/103016, 2008, A1. Location in patent: Page/Page column 7

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