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| | (1R, 2R)-2-Benzylamino-1-cyclohexanol Basic information |
| Product Name: | (1R, 2R)-2-Benzylamino-1-cyclohexanol | | Synonyms: | (1R, 2R)-2-Benzylamino-1-cyclohexanol;(1R,2R)-2-(benzylaMino)cyclohexan-1-ol;-2-(Benzylamino);(1R,2R)-2-Benzylamino-1-cyclohexanol,99%e.e.;(1R,2R)-2-BENZYLAMINO-1-CYCLOHEXANOL,MIN.98%;(1R,2R)-2-Benzylamino-1-cyclohexanol, min. 98%;Cyclohexanol, 2-[(phenylmethyl)amino]-, (1R,2R)- | | CAS: | 141553-09-5 | | MF: | C13H19NO | | MW: | 205.3 | | EINECS: | | | Product Categories: | CHIRAL CHEMICALS | | Mol File: | 141553-09-5.mol |  |
| | (1R, 2R)-2-Benzylamino-1-cyclohexanol Chemical Properties |
| storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | form | Powder | | color | white to light-yellow |
| | (1R, 2R)-2-Benzylamino-1-cyclohexanol Usage And Synthesis |
| Synthesis | General procedure for the synthesis of trans-2-benzylaminocyclohexanol from cyclohexene oxide and benzylamine: epoxycyclohexane (20 g, 204 mmol) was mixed with benzylamine (44 g, 411 mmol) and the reaction was heated for 6 hours at 80 °C. After completion of the reaction, the excess benzylamine was removed by distillation under reduced pressure. The residue was purified by silica gel column chromatography with the eluent being a chloroform solution of 5-10% methanol to give (1RS,2RS)-trans-2-benzylaminocyclohexanol (26 g, 127 mmol, 62% yield) as white crystals. | | References | [1] Tetrahedron Letters, 2008, vol. 49, # 9, p. 1546 - 1550
[2] Tetrahedron, 2011, vol. 67, # 47, p. 9214 - 9218
[3] Journal of Organic Chemistry, 2007, vol. 72, # 10, p. 3713 - 3722
[4] Tetrahedron Letters, 1990, vol. 31, # 32, p. 4661 - 4664
[5] Synthetic Communications, 2001, vol. 31, # 21, p. 3295 - 3302 |
| | (1R, 2R)-2-Benzylamino-1-cyclohexanol Preparation Products And Raw materials |
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