2-[2-(Phenylmethoxy)ethyl]cyclopentanone

Base Information

Chemical Name:2-[2-(Phenylmethoxy)ethyl]cyclopentanone
CAS No.:131685-20-6
Molecular Formula:C₁₄H₁₈O₂
Molecular Weight:218.296
Hs Code.:
DSSTox Substance ID:DTXSID801276747

Synonyms:131685-20-6;2-[2-(Phenylmethoxy)ethyl]cyclopentanone;DTXSID801276747;AKOS018122210

Suppliers and Price of 2-[2-(Phenylmethoxy)ethyl]cyclopentanone

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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 2-[2-(Phenylmethoxy)ethyl]cyclopentanone

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:218.130679813
Heavy Atom Count:16
Complexity:219

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC(C(=O)C1)CCOCC2=CC=CC=C2

Technology Process of 2-[2-(Phenylmethoxy)ethyl]cyclopentanone

There total 5 articles about 2-[2-(Phenylmethoxy)ethyl]cyclopentanone 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:

: 131685-14-8
6-(2-Benzyloxy-ethyl)-1,4-dioxa-spiro[4.4]nonane

: 131685-20-6
2-<2-(benzyloxy)ethyl>cyclopentanone

Guidance literature:: With water; pyridinium p-toluenesulfonate; In acetone; for 16h; Heating;

Reference yield:

: 54154-07-3
9-(2-hydroxyethyl)-1,4-dioxaspiro<4.4>nonane

: 131685-20-6
2-<2-(benzyloxy)ethyl>cyclopentanone

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / 50percent aq. NaOH, (n-Bu)4NHSO₄ / 0.75 h / 23 °C

2: 16.6 g / water, pyridine p-toluenesulfonate (PPTS) / acetone / 16 h / Heating

With sodium hydroxide; water; tetra(n-butyl)ammonium hydrogensulfate; pyridinium p-toluenesulfonate; In acetone;

Reference yield:

: 20826-94-2
ethyl (2-oxocyclopentyl)acetate

: 131685-20-6
2-<2-(benzyloxy)ethyl>cyclopentanone

Guidance literature:: Multi-step reaction with 4 steps

1: 86 percent / pyridine p-toluenesulfonate (PPTS) / toluene / 12 h / Heating

2: 92 percent / LiAlH₄ / diethyl ether / 1.) 0 deg C, 1 h, 2.) 23 deg C, 1 h

3: 99 percent / 50percent aq. NaOH, (n-Bu)4NHSO₄ / 0.75 h / 23 °C

4: 16.6 g / water, pyridine p-toluenesulfonate (PPTS) / acetone / 16 h / Heating

With sodium hydroxide; lithium aluminium tetrahydride; water; tetra(n-butyl)ammonium hydrogensulfate; pyridinium p-toluenesulfonate; In diethyl ether; acetone; toluene;