tert-butyl 1-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbaMate
- Product Name
- tert-butyl 1-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbaMate
- CAS No.
- 1032528-06-5
- Chemical Name
- tert-butyl 1-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbaMate
- Synonyms
- 4-[(1-BOC-Amino)cyclobutyl]phenylboronic acid pinacol ester;tert-Butyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl);tert-butyl N-{1-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutyl}carbamate;tert-butyl 1-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbaMate;Tert-butyl N-[1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutyl]carbamate;tert-Butyl 1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbamate - [B15613];[1-[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]cyclobutyl]carbamic acid tert-butyl ester;N-[1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutyl]Carbamic acid 1,1-dimethylethyl ester;CarbaMic acid, N-[1-[4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutyl]-, 1,1-diMethylethyl ester
- CBNumber
- CB32553451
- Molecular Formula
- C21H32BNO4
- Formula Weight
- 373.29
- MOL File
- 1032528-06-5.mol
tert-butyl 1-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbaMate Property
- Boiling point:
- 481.0±34.0 °C(Predicted)
- Density
- 1.08
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 11.98±0.20(Predicted)
- Appearance
- White to off-white Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- B710053
- Product name
- tert-Butyl(1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutyl)carbamate
- Packaging
- 50mg
- Price
- $130
- Updated
- 2021/12/16
- Product number
- BOR0007361
- Product name
- TERT-BUTYL-(1-(4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL)CYCLOBUTYL)CARBAMATE
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $1068.9
- Updated
- 2021/12/16
- Product number
- 090913
- Product name
- tert-Butyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxabo-rolan-2-yl)phenyl)cyclobutyl)carbamate
- Purity
- 95+%
- Packaging
- 1g
- Price
- $1311
- Updated
- 2021/12/16
- Product number
- B15613
- Product name
- tert-Butyl1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbamate
- Purity
- 95+%
- Packaging
- 5g
- Price
- $1550
- Updated
- 2021/12/16
- Product number
- BOR0007361
- Product name
- TERT-BUTYL-(1-(4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL)CYCLOBUTYL)CARBAMATE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $497.41
- Updated
- 2021/12/16
tert-butyl 1-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbaMate Chemical Properties,Usage,Production
Synthesis
1032350-06-3
73183-34-3
1032528-06-5
Step 5: In 500 mL of degassed tetrahydrofuran (THF), 27.75 g (55 mmol) of tert-butyl 1-(4-bromophenyl) cyclobutylcarbamate, 23.76 g (93.6 mmol) of pinacol ester of bis(boronic acid), 25 g (255 mmol) of potassium acetate, and 2.08 g (2.55 mmol) of 1,1 '-bis(diphenylphosphino) ferrocene palladium(II) dichloride. The reaction mixture was heated to reflux for 3 h. The color of the reaction mixture was observed to change from dark red to black. Due to incomplete reaction, heating was continued for 2 hours. Upon completion of the reaction, the reaction mixture was poured into 400 mL of water and diluted with 700 mL of ethyl acetate. After stirring for 30 minutes, the organic phase was separated and the aqueous phase was extracted twice more with 400 mL and 200 mL of ethyl acetate, respectively. The organic extracts were combined, washed with 200 mL of brine and dried with sodium sulfate. After evaporation of the solvent, the residue was purified by Biotage chromatography to afford 28.99 g (91.3% yield) of tert-butyl 1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbamate.1H NMR (400 MHz, DMSO-d6)δ: 7.51-7.67 (m, 3H), 7.38 (d, 2H), 2.22-2.42 (m, 4H), 1.88-2.02 (m, 1H), 1.63-1.80 (m, 1H), 1.00-1.38 (m, 21H) ppm.
References
[1] Patent: WO2013/104611, 2013, A1. Location in patent: Page/Page column 48
[2] Patent: WO2012/7416, 2012, A1. Location in patent: Page/Page column 75; 76
[3] Patent: US2014/5185, 2014, A1. Location in patent: Paragraph 0256-0258
[4] Patent: EP2868660, 2015, A1. Location in patent: Paragraph 0172
[5] Patent: WO2012/7345, 2012, A2. Location in patent: Page/Page column 243
tert-butyl 1-(4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutylcarbaMate Preparation Products And Raw materials
Raw materials
Preparation Products
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