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1 vote
0 answers
63 views

Amidine synthesis from nitrile and dimethylamine using n-Buli as a base

I am making LiNMe2 using n-Buli (5.5 equiv.) and dimethylamine (5.0 equiv), -15 ºC, dry THF and under nitrogen atmosphere. I have been doing the reaction and I can observe conversion of starting ...
Bree's user avatar
  • 11
1 vote
1 answer
97 views

Why is the sp3-sp3 reductive elimination between the R1 and norbornene in the Catellani Cycle ''not favorable''?

I have recently started reading a book about C-H activation and I cannot figure out why in the Catellani reaction cycle the R1-norbornene reductive elimination side reaction which can be a major issue ...
TheBorcanu's user avatar
-1 votes
1 answer
115 views

Weinreb ketone synthesis [closed]

For this problem, Can I use weinreb ketone synthesis? I found the product but not sure it is the right one If the amide react with either R1-Mgbr or R2-Li, then it produces the ketone?
user196092's user avatar
4 votes
1 answer
242 views

What is the mechanism of this reaction?

I've been stuck with this for some time. I just don't see it. As the reactant is Pd(0), I think oxidative addition will happen to the bromine. Then I would say an insertion reaction happens. However ...
Nicco's user avatar
  • 43
1 vote
0 answers
69 views

Organometallic Synthesis: Cp2Ti(I)Me from TiCl4

I've been working on this synthesis question for a couple days but I'm a little stuck. The question is: Using only $\ce{TiCl_{4}}$, $\ce{NaCp}$, $\ce{PhLi}$, $\ce{MeI}$, and $\ce{EtMgBr}$, ...
d.v.'s user avatar
  • 19
17 votes
1 answer
997 views

Are there any significant uses of the compound formed by magnesium and anthracene?

In an unusual reaction, magnesium reacts with anthracene in THF to form a grignard-like compound called, prosaically, magnesium anthracene: I remember using it briefly in the 1980s. At the time there ...
matt_black's user avatar
2 votes
0 answers
109 views

Synthesis of a tungsten carbene bromide from [CpW(CO)3]-

I'm currently working through past test and exam papers in order to prepare for my organometallic test at the end of the month, but unfortunately I've gotten stuck on the following question. Since I ...
Lenard Carroll's user avatar
3 votes
0 answers
135 views

Selectivity of olefin cross-metathesis reaction

I'm looking at the reaction shown below which uses a ruthenium catalyst: I am confused because the ruthenium catalyst which is used in the reaction should be Z selective due to the features on the ...
Jones78's user avatar
  • 79
1 vote
1 answer
5k views

Corey -House synthesis vs Wurtz reaction

In Corey House synthesis the first step is formation of Alkyl Lithium. why can't we react alkyl lithium with alkyl halide to produce alkanes. Rather we choose to prepare Gilman's reagent? Does it have ...
adi_chem's user avatar
2 votes
0 answers
102 views

Shelf Life of Methylcyclopentadiene

We are making organometallics in the lab, but instead of just regular Cyclopentadiene dimer, we crack methylcyclopentadiene dimer to make methylcyclopentadiene. I cannot find the shelf life of ...
ajs's user avatar
  • 31
19 votes
1 answer
2k views

Propose a chemical formula for the white solid that forms during the initial stages of the reaction of Sn with benzyl chloride

In my inorganic class, we carried out the synthesis of chlorotribenzyltin, $\ce{SnCl(CH2C6H5)3}$. The synthesis begins with a reflux I'll describe below: In a hood, place 2.0 g (17 mmol) of 325 mesh ...
John Snow's user avatar
  • 4,535