cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone

Base Information

Chemical Name:cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone
CAS No.:101980-84-1
Molecular Formula:C₁₇H₂₄O
Molecular Weight:244.377
Hs Code.:

Synonyms:cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone

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Technology Process of cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone

There total 3 articles about cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 75.0%

: 101980-88-5
(cis-2,2,3-trimethylcyclopentyl)(p-methylbenzyl)carbinol

: 101980-84-1
cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone

Guidance literature:: With chromic acid; In acetone;
DOI:10.1021/jo00363a020

Reference yield:

: 29875-07-8
(4-methylbenzyl)magnesium chloride

: 101980-84-1
cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether

2: 75 percent / 8 N chromic acid / acetone

With chromic acid; In diethyl ether; acetone;
DOI:10.1021/jo00363a020

Reference yield:

: 106-42-3
para-xylene

: 2767-84-2,10334-26-6,10373-78-1,71074-96-9,105309-30-6,465-29-2
Camphorquinone

: 21488-68-6
(1R)-3exo-hydroxy-bornan-2-one

: 10373-79-2,68903-65-1,101980-79-4
DL-3-endo-(4-Methyl-benzyl)-3-exo-hydroxy-bornan-2-on

: 10373-80-5,68903-64-0
DL-2-endo-(4-Methyl-benzyl)-2-exo-hydroxy-bornan-3-on

: 101980-84-1
cis-2,2,3-trimethylcyclopentyl p-methylbenzyl ketone

Guidance literature:: With hydrogen; palladium on activated charcoal; Yield given. Multistep reaction. Further byproducts given; 1.) benzene, irradiation, 2.) ethanol, RT, 1 atm;
DOI:10.1021/jo00363a020