Alternatived Products of [ 1309666-78-1 ]
Product Details of [ 1309666-78-1 ]
CAS No. : | 1309666-78-1 |
MDL No. : | MFCD22201525 |
Formula : |
C16H24O6S
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | OVLSSENVXOKYAD-UHFFFAOYSA-N |
M.W : |
344.42
|
Pubchem ID : | 60146215 |
Synonyms : |
|
Chemical Name : | tert-Butyl 3-(2-(tosyloxy)ethoxy)propanoate |
Safety of [ 1309666-78-1 ]
Application In Synthesis of [ 1309666-78-1 ]
* 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 [ 1309666-78-1 ]
- 1
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[ 104-15-4 ]
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[ 671802-00-9 ]
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[ 1309666-78-1 ]
- 2
-
[ 98-59-9 ]
-
[ 671802-00-9 ]
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[ 1309666-78-1 ]
Yield | Reaction Conditions | Operation in experiment |
55% |
With triethylamine; In tetrahydrofuran; at 0 - 20℃; for 16h; |
To a solution of Compound (g-2) (0.20 g, 1.1 mmol) and triethylamine (0.31 g, 3.2 mmol) in THF (15 mL) was added p-toluenesulfonyl chloride (0.30 g, 1.6 mmol) at 0 C. over 10 minutes, and then the reaction mixture was stirred at at room temperature 16 hours. The solvent was removed in vacuo, and the residue was purified by preparative TLC (pentane:ethyl acetate=4:1) to give Compound (h-1) (0.20 g, 55% yield). (1098) 1H-NMR (CDCl3, 400 MHz) delta: 7.71 (d, J=8.2 Hz, 2H), 7.27 (d, J=8.2 Hz, 2H), 4.07-4.05 (m, 2H), 3.55-3.54 (m, 4H), 2.39-2.33 (m, 5H), 1.36 (s, 9H). |