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CAS No. : | 125735-40-2 | MDL No. : | MFCD08062427 |
Formula : | C16H16IN | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | IBCVAYQWXMWFLD-UHFFFAOYSA-N |
M.W : | 349.21 | Pubchem ID : | 7330610 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
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 |
---|---|---|
A solution of 1-benzhydryl-3-iodoazetidine 13a (1.4 mmol, 490 mg) in 5 mL of THF was added to a stirring mixture of SmI2 (0.1 M THF solution, 3 mmol, 30 mL) and 1.7 mL of HMPA. After 5 min, a solution of 1-benzoylpiperidin-4-one 13b (3.1 mmol, 626 mg) in 5 mL of THF was added. The reaction mixture was stirred for 2 h. Saturated aqueous NH4Cl solution (20 mL) was added and the suspension was filtered through a diatomaceous earth pad. The solids were washed with chloroform and the combined organic layers were washed with brine, dried, and concentrated. The crude residue was purified by preparative reverse-phase chromatography to give 400 mg (55percent yield) of compound 13c (mono-TFA salt) as a yellow oil. MS m/z 401.2 (M+H+). |
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