Name | 3-(tert-Butoxycarbonyl)phenylboronic acid |
Synonyms | T-BUTYL 3-BORONOBENZOATE 3-(Tert-Butoxycarbonyl)Phenylb 3-(T-BUTOXYCARBONYL)PHENYLBORONIC ACID 3-tert-Butoxycarbonylphenylboronicacid 3-tert-Butoxycarbonylphenylboronic acid 3-(T-BUTOXYCARBONYL)PHENYLBORBONIC ACID 3-(tert-Butoxycarbonyl)phenylboronic acid 3-(TERT-BUTOXYCARBONYL)PHENYLBORONIC ACID 3-(TERT-BUTOXYCARBONYL)BENZENEBORONIC ACID [3-[(2-methylpropan-2-yl)oxy-oxomethyl]phenyl]boronic acid |
CAS | 220210-56-0 |
EINECS | 691-957-9 |
InChI | InChI=1/C11H15BO4/c1-11(2,3)16-10(13)8-5-4-6-9(7-8)12(14)15/h4-7,14-15H,1-3H3 |
Molecular Formula | C11H15BO4 |
Molar Mass | 222.05 |
Density | 1.15±0.1 g/cm3(Predicted) |
Melting Point | 96-102°C |
Boling Point | 375.0±44.0 °C(Predicted) |
Flash Point | 180.6°C |
Solubility | soluble in Methanol |
Vapor Presure | 2.74E-06mmHg at 25°C |
Appearance | powder to crystal |
Color | White to Almost white |
pKa | 7.72±0.10(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Refractive Index | 1.517 |
Use | This product is for scientific research only and shall not be used for other purposes. |
Hazard Symbols | Xi - Irritant![]() |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S60 - This material and its container must be disposed of as hazardous waste. S37 - Wear suitable gloves. |
HS Code | 29319000 |
Hazard Note | Irritant/Keep Cold |
application | 3-(tert-butoxycarbonyl)-phenylboronic acid can be used as an intermediate in organic synthesis and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process. |
prepare | 10L glass reactor with mechanical stirring, thermometer and constant pressure dropping funnel, add 3 moles of raw material m-carboxyphenylboronic acid and 4kg of tetrahydrofuran under nitrogen protection, add 4.5 moles of sulfoxide chloride dropwise under reflux stirring, react for 4 hours, cool down to 0-5 ℃, add 7.5 moles of potassium tert-butoxide in batches, and continue stirring for 1 hour after adding, add 2kg of water, acidify with acetic acid, stand still, and separate liquid. The organic phase was concentrated to obtain crude product, and 2kg of petroleum ether was added to recrystallize to obtain solid product 3-(tert-butoxycarbonyl)-phenylboronic acid with 98% purity and 95% molar yield. |