Benzyl 2-Hydroxy-2-Methylpropionate
- Product Name
- Benzyl 2-Hydroxy-2-Methylpropionate
- CAS No.
- 19444-23-6
- Chemical Name
- Benzyl 2-Hydroxy-2-Methylpropionate
- Synonyms
- Benzyl 2-hydroxy-2-methylpropanoate;Benzyl 2-Hydroxy-2-Methylpropionate;2-Propenoicacid,2-(4-hydroxyethoxy)ethylester
- CBNumber
- CB32597037
- Molecular Formula
- C11H14O3
- Formula Weight
- 194.22706
- MOL File
- 19444-23-6.mol
Benzyl 2-Hydroxy-2-Methylpropionate Property
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- Colorless to light yellow Liquid
Safety
- HS Code
- 2918199890
N-Bromosuccinimide Price
- Product number
- B288708
- Product name
- Benzyl2-Hydroxy-2-methylpropionate
- Packaging
- 500mg
- Price
- $175
- Updated
- 2021/12/16
- Product number
- CS-0060866
- Product name
- Benzyl2-hydroxy-2-methylpropanoate
- Packaging
- 1g
- Price
- $94
- Updated
- 2021/12/16
- Product number
- 6533AJ
- Product name
- Benzyl2-hydroxy-2-methylpropionate
- Packaging
- 250mg
- Price
- $104
- Updated
- 2021/12/16
- Product number
- 6533AJ
- Product name
- Benzyl2-hydroxy-2-methylpropionate
- Packaging
- 1g
- Price
- $171
- Updated
- 2021/12/16
- Product number
- CS-0060866
- Product name
- Benzyl2-hydroxy-2-methylpropanoate
- Packaging
- 5g
- Price
- $290
- Updated
- 2021/12/16
Benzyl 2-Hydroxy-2-Methylpropionate Chemical Properties,Usage,Production
Uses
Benzyl 2-Hydroxy-2-methylpropionate is a useful chemical in organic synthesis.
Synthesis
594-61-6
100-39-0
19444-23-6
To a solution of 2-hydroxy-2-methylpropionic acid (500 mg, 4.80 mmol) in anhydrous tetrahydrofuran (THF, 10 ml) was added sodium hydride (NaH, 60% mineral oil dispersion, 192 mg, 4.80 mmol) batchwise at 5 °C. The reaction mixture was stirred at room temperature for 1 hour. The solvent was removed under reduced pressure and the residue was suspended in anhydrous N,N-dimethylformamide (DMF, 7 ml), followed by the addition of benzyl bromide (821 mg, 4.80 mmol) and a catalytic amount of potassium iodide (KI). The reaction mixture was placed in a microwave reactor and heated at 100 °C for 3 hours. After completion of the reaction, it was cooled to room temperature and the solvent was removed by evaporation under reduced pressure. The residue was dissolved in a solvent mixture of water and ethyl acetate (EtOAc) for partition extraction. The organic phase was separated, washed with saturated saline, dried over anhydrous sodium sulfate, filtered and concentrated to dryness under reduced pressure. The residue was purified by rapid chromatography on silica gel column (eluent: ethyl acetate/petroleum ether=1/1, v/v) to afford benzyl 2-hydroxy-2-methylpropionate as yellow liquid (773 mg, 3.98 mmol, 83% yield).
References
[1] Tetrahedron, 2001, vol. 57, # 20, p. 4323 - 4336
[2] Patent: US2008/9474, 2008, A1. Location in patent: Page/Page column 19
[3] Patent: US2013/79313, 2013, A1. Location in patent: Paragraph 1009
[4] Patent: WO2009/73138, 2009, A2. Location in patent: Page/Page column 81
[5] Bioorganic and Medicinal Chemistry Letters, 1999, vol. 9, # 11, p. 1541 - 1546
Benzyl 2-Hydroxy-2-Methylpropionate Preparation Products And Raw materials
Raw materials
Preparation Products
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