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| | 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 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 | | pka | 9.44±0.20(Predicted) | | form | solid | | color | white to pale yellow | | InChI | 1S/C5H9BO2/c7-6(8)5-3-1-2-4-5/h3,7-8H,1-2,4H2 | | InChIKey | UZBHNSVUMGIKLU-UHFFFAOYSA-N | | SMILES | OB(O)C1=CCCC1 |
| 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 Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Dermal Acute Tox. 4 Inhalation Acute Tox. 4 Oral Eye Dam. 1 Skin Irrit. 2 STOT SE 3 |
| | CYCLOPENTEN-1-YLBORONIC ACID Usage And Synthesis |
| Chemical Properties | Off-white powder | | Uses | suzuki 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%.
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| | CYCLOPENTEN-1-YLBORONIC ACID Preparation Products And Raw materials |
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