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CAS No. : | 92511-12-1 | MDL No. : | MFCD01863695 |
Formula : | C10H23IOSi | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | INGJYKISFRSCQV-UHFFFAOYSA-N |
M.W : | 314.28 | Pubchem ID : | 4250746 |
Synonyms : |
|
Chemical Name : | tert-Butyl(4-iodobutoxy)dimethylsilane |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302 | Packing Group: | N/A |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
67% | With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 - 20℃; for 18.5h; | Benzyl 4-(4-(tert-butyldimethylsilyloxy)butyl)-4-cyanopiperidine-1-carboxylate. To a stirred solution of <strong>[161609-84-3]benzyl 4-cyanopiperidine-1-carboxylate</strong> (10 g, 410 mmol) and iodo-tert-butyldimethylsilane butane (12.6 mL, 49 mmol) in THF (80 mL) cooled to -78 C. was added LiHMDS (50 mL, 50 mmol, 1M in THF) dropwise over 30 min. The resulting mixture was stirred while gradually warming to room temperature for 18 h. After quenching with water, the organic phase was diluted with EtOAc and washed with water, brine and dried (Na2SO4). After concentration, the residue was purified by flash chromatography (1% to 20% EtOAc/hexane) to give the title compound as yellow oil (11.88 g, 67% yield). 1H NMR (300 MHz, CDCl3) delta: 7.34-7.28 (5H, m), 5.09 (2H, s), 4.17 (2H, bs), 3.59 (2H, t, J=5.3 Hz), 3.07 (2H, bs), 1.89 (2H, d, J=13.2 Hz), 1.53 (6H, bs), 1.43-1.34 (2H, m), 0.85 (9H, s), 0.01 (6H, s). LCMS (M+H): 431.20. |
[ 78878-05-4 ]
tert-Butyl(3-iodopropoxy)dimethylsilane
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