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Chemical Structure| 936691-31-5 Chemical Structure| 936691-31-5

Structure of 936691-31-5

Chemical Structure| 936691-31-5

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Product Details of [ 936691-31-5 ]

CAS No. :936691-31-5
Formula : C10H18BrNOSSi
M.W : 308.31
SMILES Code : C[Si](C(C)(C)C)(C)OCC1=CSC(Br)=N1
MDL No. :MFCD26399018

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Application In Synthesis of [ 936691-31-5 ]

* 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 [ 936691-31-5 ]

[ 936691-31-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 850568-54-6 ]
  • [ 936691-31-5 ]
  • tert-butyl 4-(4-(((tert-butyldimethylsilyl)oxy)methyl)thiazol-2-yl)benzoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
53% With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; sodium carbonate; In toluene; tert-butyl alcohol; at 95℃; for 6h;Sealed tube; A mixture of 2-bromo-4-(((tert-butyldimethylsilyl)oxy)methyl)thiazole (1.542 g, 5.000 mmol) and <strong>[850568-54-6](4-(tert-butoxycarbonyl)phenyl)boronic acid</strong> (1.388 g, 6.25 mmol) in toluene:terti-butanol (3:1, 60 mL) was purged with a stream of nitrogen bubbles in a sealable flask for 15 min. To this mixture was added Pd(dppf)Cl2.DCM (204 mg, 0.250 mmol) and 2 M Na2C03 (3.13 mL, 6.25 mmol), the flask was sealed and the mixture was stirred at 95 °C (oil bath temperature) for 4 h. Another 0.25 equiv of the boronic acid and 2 M Na2C03 was then added, together with an arbitrary but small amount of the catalyst. The mixture was stirred at 95 °C for another 2 h and then the cooled mixture was partitioned with EtOAc-water. The organic phase was separated, washed with brine, dried over Na2S04 and evaporated to give a dark brown gum. Flash chromatography on the ISCO (0-10percent EtOAc-hexane) afforded the title compound (1.065 g, 53percent) as a colorless gum. LC (Method B): 3.407 min. MS (APCI): calcd for C2iH32N03SSi [M+H]+ m/z, 406.19, found 406.2. 1HNMR (400 MHz, CDC13) delta ppm 8.04 (d, J = 8.6 Hz, 2H), 7.98 (d, J = 8.6 Hz, 2H), 7.26 (s, 1H), 4.79 (s, 2H), 1.47 (s, 9H), 0.82 (s, 9H), 0.10 (s, 6H).
52.5% A mixture of 2-bromo-4-(((tert-butyldimethylsilyl)oxy)methyl)thiazole (Example 37B, 1.542 g, 5.000 mmol) and (4-(tert-butoxycarbonyl)pfienyl)boronic acid (1.388 g, 6.25 mmol) in toluene-tert-butanol (3: 1, 60 mL) was purged with a stream of N2 bubbles for 15 min in a sealable flask. To this mixture was added Pd(dppf)Cl2.DCM (0.204 g, 0.250 mmol) and 2 M Na2C03 (3.13 mL, 6.25 mmol), the flask was sealed and the mixture was stirred at 95 °C (oil bath temperature) for 4 h. Another 0.25 equiv of the boronic acid and 2 M Na2CO3 were added, together with a small amount of the catalyst. The mixture was heated at 95 °C for another 2 h before being allowed to cool to room temperature and then partitioned with EtO Ac-water. The organic phase was separated, washed (brine), dried (Na2S04) and evaporated to give a dark brown gum. Flash chromatography (Isco/ 0-10percent EtOAc-hexane) of this gum afforded the title compound (1.065 g, 52.5percent) as a colorless gum. This material was used as such in the next step. LC (Method B): 3.407 min. LCMS (APCI): calcd for C21H32N03SSi [M+H]+ m/z 406.19; found 406.2. 1H NMR (400 MHz, CDCl3) delta ppm: 8.04 (d, J= 8.6 Hz, 2H), 7.98 (d, J= 8.6 Hz, 2H), 7.26 (s, 1H), 4.79 (s, 2H), 1.47 (s, 9H), 0.82 (s, 9H), 0.10 (s, 6H).
  • 2
  • [ 22929-52-8 ]
  • [ 936691-31-5 ]
  • 3-(4-(((tert-butyldimethylsilyl)oxy)methyl)thiazol-2-yl)tetrahydrofuran-3-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
66.7% A solution of 2-bromo-4-(((tert-butyldimethylsilyl)oxy)methyl)thiazole (Example 37B, 1.542 g, 5.000 mmol) in dry THF (20 mL) was cooled at -78 °C under N2 and then 1.45 M n-butyllithium (3.79 mL, 5.50 mmol) was added dropwise. The resulting mixture was stirred for 15 min to give a pale yellow-brown solution. To this mixture was slowly added a solution of <strong>[22929-52-8]dihydrofuran-3(2H)-one</strong> (0.517 g, 6.00 mmol) in dry THF (2.5 mL) and the mixture was stirred at -78 °C for 1 h, to give a light brown solution. The reaction was then quenched by the addition of saturated aqueous NH4Cl (5 mL), the cooling bath was removed and the mixture was partitioned with EtO Ac-water. The organic phase was separated, washed (brine), dried (Na2S04) and evaporated to give a pale yellow oil. Flash chromatography (Isco/ 0-50percent EtOAC-hexane) afforded 3-(4- (((tert-butyldimethylsilyl)oxy)methyl)thiazol-2-yl)tetrahydrofuran-3-ol (1.052 g, 66.7percent>) as an oil which crystallized on standing in vacuo. This material was used as such in the next step. LC (Method A): 2.226 min. HRMS(ESI): calcd for C14H26NO3SSi [M+H]+ m/z 316.140; found 316.147. 1H NMR (400 MHz, DMSO-d6): delta 7.28 (s, 1H), 6.32 (s, 1H), 4.65 (s, 2H), 3.92 (m, 2H), 3.78 (q, J= 9.00 Hz, 2H), 2.36 (dt, J= 9.00, 12.52 Hz, 1H), 2.09 (dt, J= 5.09, 12.52 Hz, 1H), 0.82 (s, 9H), 0.00 (s, 6H).
 

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