Application of exo-3-Azabicyclo[3.1.0]hexan-6-ylmethanol

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 134575-13-6, exo-3-Azabicyclo[3.1.0]hexan-6-ylmethanol.

Synthetic Route of 134575-13-6, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 134575-13-6, name is exo-3-Azabicyclo[3.1.0]hexan-6-ylmethanol. This compound has unique chemical properties. The synthetic route is as follows.

(1R,5S,6R)-3-Azabicyclo[3.1.0]hexan-6-ylmethanol 31a (10 g, 88.4 mmol) was dissolved in a mixed solvent of dioxane and H2O (V/V=3/2), followed by addition of sodium hydroxide (4.2 g, 106 mmol) and di-tert-butyl dicarbonate (28.9 g, 132.6 mmol). After reacting for 10 hours, 50 mL of H2O was added to the reaction mixture. The reaction mixture was extracted with ethyl acetate (150 mLx3). The organic phases were combined, washed with saturated sodium chloride solution (50 mLx2), dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography with elution system C to obtain the title product (1R,5S,6R)-tert-butyl 6-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate 31b (16.9 g, yield 89.9%) as a light yellow liquid.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 134575-13-6, exo-3-Azabicyclo[3.1.0]hexan-6-ylmethanol.

Reference:
Patent; Zhang, Xuejun; Dong, Qing; Liu, Bonian; Zhu, Yaoping; Li, Xiaotao; Lan, Jiong; US2014/336207; (2014); A1;,
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