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OpenStudy (spitfire77):

Help with reaction

OpenStudy (spitfire77):

|dw:1431489682127:dw|

OpenStudy (spitfire77):

|dw:1431489813840:dw|

OpenStudy (spitfire77):

What is a reaction to get this?

rvc (rvc):

Phenol + aryl halide

OpenStudy (spitfire77):

Im confused on how after the br and oh react to create the ether it goes to a keytone

rvc (rvc):

just wait a sec let me check i dont remember exactly

OpenStudy (spitfire77):

np, and thank you

OpenStudy (spitfire77):

ketone*

rvc (rvc):

i think its electrophilic reaction

rvc (rvc):

what are the reagents?

rvc (rvc):

@chmvijay please help :) @Somy

OpenStudy (spitfire77):

any can be used, but i must start with those two^

OpenStudy (spitfire77):

Is there a common reagent for changing ethers to ketones?

rvc (rvc):

well i forget the stuff XD

OpenStudy (spitfire77):

I appreciate the help though!

OpenStudy (spitfire77):

Thank if you are coming from reddit/r/chemhelp

rvc (rvc):

atm im busy with my tutorial stuff im sorry

OpenStudy (spitfire77):

think i may have found it, can someone check?

OpenStudy (spitfire77):

maybe it is supposed to start as the Br-R(1) and you could add the phenol, or change it somehow to an benzaldehyde with DMP then add Mg... making a grignard addition and then finally adding dmp again to change the OH to a =O

OpenStudy (spitfire77):

Br-R(1) is the R group it starts with

OpenStudy (aaronq):

|dw:1431534331691:dw|

OpenStudy (aaronq):

then grignard

OpenStudy (jimdemers):

I'm pretty sure the first starting material is supposed to be benzyl alcohol, PhCH2OH, and not phenol (Ph-OH). If I'm right about that, you need to (1) oxidize it to benzaldehyde (PHCHO), add a Grignard reagent made from the 3-bromothiophene, and then oxidize the resulting alcohol to the ketone.

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