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CYCLOPENTEN-1-YLBORONIC ACID

CYCLOPENTEN-1-YLBORONIC ACID Suppliers list
Company Name: future industrial shanghai co., ltd  
Tel: 400-0066400 13621662912
Email: sales@jonln.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: TCI (Shanghai) Development Co., Ltd.  
Tel: 021-67121386
Email: Sales-CN@TCIchemicals.com
Company Name: BeiJing Hwrk Chemicals Limted  
Tel: 0757-86329057 18934348241
Email: sales4.gd@hwrkchemical.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com

CYCLOPENTEN-1-YLBORONIC ACID manufacturers

CYCLOPENTEN-1-YLBORONIC ACID Basic information
Product Name:CYCLOPENTEN-1-YLBORONIC ACID
Synonyms:1-Cyclopentenylboronic Acid (contains varying amounts of Anhydride);Cyclopentenylboronic acid;1-CYCLOPENTEN-1-YLBORONIC ACID;Cyclopent-1-ene-1-boronic acid;CYCLOPENTEN-1-YLBORONIC ACID;Cyclopentene-1-boronic acid, 97%;1-Boronocyclopent-1-ene;Boronic acid,B-1-cyclopenten-1-yl-
CAS:850036-28-1
MF:C5H9BO2
MW:111.93
EINECS:
Product Categories:blocks;BoronicAcids
Mol File:850036-28-1.mol
CYCLOPENTEN-1-YLBORONIC ACID Structure
CYCLOPENTEN-1-YLBORONIC ACID Chemical Properties
Melting point 134-140°C
Boiling point 246.7±33.0 °C(Predicted)
density 1.08±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka9.44±0.20(Predicted)
form solid
color white to pale yellow
InChI1S/C5H9BO2/c7-6(8)5-3-1-2-4-5/h3,7-8H,1-2,4H2
InChIKeyUZBHNSVUMGIKLU-UHFFFAOYSA-N
SMILESOB(O)C1=CCCC1
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-41-37/38
Safety Statements 26-36/37/39-39
WGK Germany WGK 3
Hazard Note Harmful/Irritant/Keep Cold
TSCA No
HS Code 29319090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
CYCLOPENTEN-1-YLBORONIC ACID Usage And Synthesis
Chemical PropertiesOff-white powder
Usessuzuki reaction
Synthesis

Cyclopenten-1-ylboronic acid is prepared as follows:

The first step of the raw material 1-chlorocyclopentene preparation: to a 2L four-necked bottle equipped with magnetic stirring, thermometer, condenser tube and exhaust gas alkali absorption device, add 374.2 (1.818mol, 1.05) phosphorus pentachloride, 863g of n-heptane, warming to 70 , drop 151.4g (1.803mol, 1eq) cyclopentanone, about 2 hours after the drop, and continue the reaction Half an hour, after cooling down to 0 , dropwise addition of 6 mol / L sodium hydroxide solution 0.69 kg, stirring for one hour, separation of the upper organic layer, the organic layer was washed once with saturated sodium bicarbonate, to obtain 1-chlorocyclopentene n-hexane solution 799 g, the internal standard yield of 81.1%;

The second step of preparation of cyclopenten-1-ylboronic acid: to a 5L four-necked flask equipped with mechanical stirring, thermometer, argon protection and reflux condenser tube was added T2215.5g (1.608mol, 1.1eq), lithium metal 22.6g (3.216mol, 2.2eq), tetrahydrofuran 678g, cooled down to -10C, and dropwise addition of 1-chlorocyclopentene's Heptane solution (1eq), titration is completed insulation -10 stirring 11 hours, GC control, the end of the reaction, add 1.3kg6N hydrochloric acid adjust PH = 2 ~ 3, stratification, the aqueous layer and then 400g of ethyl acetate extracted once, combined with the organic layer, 40 distillation under reduced pressure, to not flow, precipitation of solids, add 200g of n-heptane-10 pulp, filtration, drying to obtain the white solid cyclopentene -1-ylboronic acid 89.3g, yield 54.5%.

CYCLOPENTEN-1-YLBORONIC ACID Preparation Products And Raw materials
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