Would adding phosgene to ortho-xylene lead to the formation of 2-indanone?

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    $\begingroup$ I don't think so. Also, you should avoid phosgene like the plague. It will kill you faster than that. How about just buying it? $\endgroup$ – Zhe Dec 23 '16 at 21:41
  • $\begingroup$ orgsyn.org/demo.aspx?prep=CV5P0647.. this might help you.. if there is any confusion or want the proper answer.... plz comment. i would be writing the procudure clearly.. $\endgroup$ – CCR Dec 24 '16 at 4:15

If you want to start from ortho-xylene 1 I would recommend dibromination using N-bromosuccinimide to obtaining ortho-di(bromomethyl)benzene 2, followed by the addition of 1,3-dithianide anion 3 (prepared from formaldehyde and 1,2-ethanedithiol followed by treatment with NaH). While formaldehyde is electrophylic, 1,3-dithiane is nucleophylic if deprotonated (eg. with NaH, forming 1,3-dithianide ion) and can attack on the bromomethyl side of the molecule to get 4. This polarity inversion is called umpolung. A second treatment with NaH gives the cyclized product 5. Deprotection of the thioacetal gives 2-indanone 6. With this reversed polarity approach no phosgene is needed for the synthesis.

a synthesis of 2-indanone from o-xylene using an umpolung approach described in the paragraph above[1]

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    $\begingroup$ Care would need to be taken in the NBS reaction. NBS is also a source of electrophilic bromine and will brominate activated aromatic rings in polar solvents (personal experience). $\endgroup$ – Ben Norris Dec 24 '16 at 20:11
  • $\begingroup$ 1,3-ditianide?? $\endgroup$ – Prakhar Dec 25 '16 at 4:49
  • $\begingroup$ @Tetrahydrocannabinol Yes, it is the dithioacetal of formaldehyde. While formaldehyde is electrophylic, 1,3-dithiane is nucleophylic if deprotonated (eg. with NaH, forming 1,3-dithianide ion) and can attack on the bromomethyl side of the molecule. This polarity inversion is called umpolung. If you are not familiar with it I suggest you to look it up, because it is very interesting and useful. $\endgroup$ – fazekaszs Dec 25 '16 at 7:47
  • $\begingroup$ If memory serves me correctly, the anion 3 of 1,3-dithiolane undergoes fragmentation. That is why 1,3-dithiane is used. $\endgroup$ – user55119 Sep 22 '19 at 19:03

If you need to start with ortho-xylene, then you should use fazekazs's approach. I searched through SciFinder and found that the most commonly reported synthesis of 2-indanone involves oxidation of indene using a variety of conditions.

The following Organic Synthesis prep highlights this approach, although it certainly uses some outdated methodology (distillation by aspirator vs. rotary evaporation, for example). Newer reports use a variety of oxidations, including oxone or the the Wacker process.

In this example, indene 1 is added to a mixture of formic acid and hydrogen peroxide to afford the monoformate ester of indene 1,2-diol 2. The monoformate ester was hydrolyze with sulfuric acid to give 2-indanone 3.

A synthesis of 2-indanone by oxidation of indene

However, when I first saw your question, I wanted to propose a synthesis based on a Dieckmann condensation on diethyl phenylene-1,2-diacetate 4 followed by decarboxylation of the $\beta$-ketoester 5. However, I did not find this approach in the literature, and both the diacetate ester and its parent diacid are of comparaple price to 2-indanone.

synthesis of 2-indanone by a Dieckmann condensation

Another interesting idea that I did not find in the literature is a pericyclic approach based on photolysis or thermolysis of beznocyclobutene 5 in the presence of carbon monoxide. Following electrocyclic ring opening, intermediate 6 can react with CO in 4+1 cycloaddition. An isocyanide could be used instead of CO, and hydrolysis of the imine would give 2-indanone. Alternatively, there may be a transition metal species that could mediate this transformation.

A synthesis of 2-indnaone via pericyclic reactions

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