[1-(4-Chlorophenyl)-2-oxopropyl] acetate

Base Information

Chemical Name:[1-(4-Chlorophenyl)-2-oxopropyl] acetate
CAS No.:56955-39-6
Molecular Formula:C₁₁H₁₁ClO₃
Molecular Weight:226.66
Hs Code.:
DSSTox Substance ID:DTXSID901257641
Nikkaji Number:J3.237.585E

Synonyms:56955-39-6;DTXSID901257641;1-(Acetyloxy)-1-(4-chlorophenyl)-2-propanone

Suppliers and Price of [1-(4-Chlorophenyl)-2-oxopropyl] acetate

Supply Marketing:

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

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Chemical Property of [1-(4-Chlorophenyl)-2-oxopropyl] acetate

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:226.0396719
Heavy Atom Count:15
Complexity:244

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)C(C1=CC=C(C=C1)Cl)OC(=O)C

Technology Process of [1-(4-Chlorophenyl)-2-oxopropyl] acetate

There total 5 articles about [1-(4-Chlorophenyl)-2-oxopropyl] acetate 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: 96.0%

: 7342-10-1
1-(4-chlorophenyl)prop-2-yn-1-yl acetate

: 56955-39-6
1-(4-chlorophenyl)-2-oxopropyl acetate

Guidance literature:: With silver hexafluoroantimonate; C₂₀H₂₄AuClN₂; water; In acetonitrile; at 20 ℃; for 3h;
DOI:10.1021/om4002928

Reference yield:

: 1041849-95-9,1132664-68-6
1-(4-chlorophenyl)-3-(trimethylsilyl)prop-2-yn-1-ol

: 56955-39-6
1-(4-chlorophenyl)-2-oxopropyl acetate

Guidance literature:: Multi-step reaction with 3 steps

1: methanol; potassium carbonate / 12 h / 20 °C / Inert atmosphere

2: dmap; triethylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere

3: chloro(triphenylphosphine)gold(I); F₅Sb*AgF; water / 1,4-dioxane / 5 h / 20 °C / Inert atmosphere

With methanol; dmap; chloro(triphenylphosphine)gold(I); F₅Sb*AgF; water; potassium carbonate; triethylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1021/jo101995g

Reference yield:

: 29805-11-6
1-(4-chlorophenyl)prop-2-yn-1-ol

: 56955-39-6
1-(4-chlorophenyl)-2-oxopropyl acetate

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; triethylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere

2: chloro(triphenylphosphine)gold(I); F₅Sb*AgF; water / 1,4-dioxane / 5 h / 20 °C / Inert atmosphere

With dmap; chloro(triphenylphosphine)gold(I); F₅Sb*AgF; water; triethylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1021/jo101995g