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| | 2-BROMO-5-HYDROXYMETHYL-ANISOLE Basic information |
| Product Name: | 2-BROMO-5-HYDROXYMETHYL-ANISOLE | | Synonyms: | 2-BROMO-5-HYDROXYMETHYL-ANISOLE;4-Bromo-3-methoxybenzyl alcohol;Benzyl alcohol, 4-bromo-3-methoxy-;Benzenemethanol, 4-bromo-3-methoxy-;(4-broMo-3-Methoxyphenyl)Methanol | | CAS: | 17100-64-0 | | MF: | C8H9BrO2 | | MW: | 217.06 | | EINECS: | | | Product Categories: | | | Mol File: | 17100-64-0.mol |  |
| | 2-BROMO-5-HYDROXYMETHYL-ANISOLE Chemical Properties |
| Boiling point | 306.8±27.0 °C(Predicted) | | density | 1.513±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | pka | 14.04±0.10(Predicted) | | form | solid | | color | Faint orange/brown |
| | 2-BROMO-5-HYDROXYMETHYL-ANISOLE Usage And Synthesis |
| Synthesis | The general procedure for the synthesis of 2-bromo-5-hydroxymethyl anisole from m-methoxybenzyl alcohol was as follows: to a solution of 3-methoxybenzyl alcohol (20.0 g, 145 mmol) in tetrahydrofuran (THF, 400 mL) was added N-bromosuccinimide (NBS, 26 g, 146 mmol). The reaction mixture was stirred at room temperature for 8 hours. After the reaction was completed, ether (500 mL) was added to dilute and the mixture was washed with deionized water (3 x 100 mL). The organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford 2-bromo-5-hydroxymethyl anisole (31.2 g, 99% yield), and the product was used directly in the next reaction without further purification. | | References | [1] Patent: US9725406, 2017, B1. Location in patent: Page/Page column 7-8
[2] Tetrahedron, 2005, vol. 61, # 49, p. 11692 - 11696
[3] Patent: US2018/208604, 2018, A1. Location in patent: Paragraph 0201-0203
[4] Patent: US2010/4159, 2010, A1. Location in patent: Page/Page column 59; 64
[5] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 3, p. 1010 - 1014 |
| | 2-BROMO-5-HYDROXYMETHYL-ANISOLE Preparation Products And Raw materials |
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