Adding a certain compound to certain chemical reactions, such as: 3840-31-1, (3,4,5-Trimethoxyphenyl)methanol, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, Safety of (3,4,5-Trimethoxyphenyl)methanol, blongs to alcohols-buliding-blocks compound. Safety of (3,4,5-Trimethoxyphenyl)methanol
i 3,4,5-Trimethoxybenzyl chloride In 40 ml of benzene was dissolved 10 g of 3,4,5-trimethoxybenzyl alcohol. To the resulting solution was dropwise added under chilling with ice 10 ml of benzene solution containing 7.6 g of thionyl chloride. After the addition was complete, the mixture was stirred at room temperature for 15 min. The reaction solution was poured into a chilled aqueous potassium carbonate, and a separated benzene portion was collected. The benzene portion was washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and placed under reduced pressure to distill off the solvent. The desired compound was obtained as a yellow solid (yield: 11.0 g).
The synthetic route of 3840-31-1 has been constantly updated, and we look forward to future research findings.
Reference:
Patent; Nippon Chemiphar Co., Ltd.; US5070089; (1991); A;,
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