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Chemical Structure| 180046-62-2 Chemical Structure| 180046-62-2

Structure of 180046-62-2

Chemical Structure| 180046-62-2

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Product Details of [ 180046-62-2 ]

CAS No. :180046-62-2
Formula : C14H30O2Si
M.W : 258.47
SMILES Code : CC(C)(C)[Si](C)(C)OC[C@H]1CC[C@H](CO)CC1
MDL No. :MFCD28403619

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Application In Synthesis of [ 180046-62-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 180046-62-2 ]

[ 180046-62-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3236-48-4 ]
  • [ 18162-48-6 ]
  • [ 180046-62-2 ]
YieldReaction ConditionsOperation in experiment
62% With 1H-imidazole; In DMF (N,N-dimethyl-formamide); at 25℃; for 16h; To a 100 mL-flask containing 79 (4.0 g, 27.8 mmol) in DMF (40 mL) was added TBDMSCl (3.56 g, 23.6 mmol) and imidazole (3.79 g, 55.6 mmol). The reaction was allowed to stir at 25 C. for 16 hours after which time saturated aqueous LiBr (50 mL) was added and the reaction extracted with ether (2×50 mL). The ether layers were pooled and extracted again with LiBr (2×35 mL). The ether layer became clear. The ether layer was then concentrated in vacuo and the product purified by flash chromatography, on a silica gel column, eluting with 1:2 ether/petroleum ether to yield 83 (3.80 g, 62%) as a homogenous oil. 1H NMR (CDCl3) delta 3.46 (d, J=6.2 Hz, 2H), 3.39 (d, J=6.2 Hz, 2H), 1.95-1.72 (m, 4H), 1.65 (m, 1H), 1.40 (m, 1H), 1.03-0.89 (m, 4H), 0.88 (s, 9H), 0.04 (s, 6H); 13C NMR (CDCl3) delta 69.2, 69.1, 41.2, 41.1, 29.5, 26.5, 18.9, -4.8; APCI m/z (rel intensity) 259 (MH+, 100).
45.1% With 1H-imidazole; In N,N-dimethyl-formamide; at 0 - 25℃; for 16h; To a 500-mL flask containing(lR,4R)-cyclohexane-l,4-diyldimethanol (80 g, 555 mmol) and 1H- imidazole (37.8 g, 555 mmol) in DMF (400 mL) was added to a solution of tert- butylchlorodimethylsilane (84 g, 555 mmol) in DMF (400 mL) at about 0C. After addition, the reaction was allowed to stir at about 25C for about 16 h. The solution was poured into ice water (200 mL) and extracted with MTBE (3x100 mL). The organics were combined, concentrated in vacuo, and purified by flash chromatography on silica gel (1 :2 EtOAc/petroleum ether) to afford the title compound (68 g, 45.1 %); lH NMR (400MHz, CDC13) delta 0.03 (s, 6 H) 0.86 - 0.96 (m, 13 H) 1.34 - 1.58 (m, 3 H) 1.81 (d, J=8.61 Hz, 4 H) 3.42 (dd, J=17.61, 6.26 Hz, 4 H)
With 1H-imidazole; In N,N-dimethyl-formamide; To a solution of trans-<strong>[3236-48-4]1,4-cyclohexanedimethanol</strong> (3.46 g, 24.0 mmol) in DMF (40 ml) was added ten?butyldimethylsilyl chloride (3.01 g, 20 mmol) and imidazole (3.27 g, 48.0 mmol). The reaction was allowed to stir overnight. The reaction was then partitioned between ether and brine. The organic layer was separated, washed with brine, dried over sodium sulfate,filtered and evaporated. The crude product was purified on a Biotage 40M silica gel column, eluting with a gradient of 10-50% ethyl acetate in hexanes to give the title compound. NMRo (ppm)(CDCl3): 3.46 (d, 2H), 3.40 (d, 2H), 1.81 (m, 4H), 1.42 (m, 2H), 1.26 (s, 1H), 0.94 (m, 4H), 0.89 (s, 9H), 0.03 (s, 6H).
  • 2
  • [ 180046-62-2 ]
  • [ 3236-48-4 ]
YieldReaction ConditionsOperation in experiment
96% With sodium tetrachloroaurate(III) dihydrate; In methanol; at 20℃; for 2h; General procedure: A solution of the TBS ether (2 mmol) in MeOH (4 mL) was treated with NaAuCl4·2H2O (4.0 mg, 0.01 mmol, 0.005 equiv) at r.t. When the starting material had disappeared (TLC), mixture was diluted with EtOAc (10 mL) and filtered through activated alumina. The solution was then concentrated in vacuo and the resulting residue was purifiedby flash column chromatography.
 

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