1-Propanone, 2,2-difluoro-1-(4-methoxyphenyl)-

Base Information

• Chemical Name: 1-Propanone, 2,2-difluoro-1-(4-methoxyphenyl)-
• CAS No.: 144464-70-0
• Molecular Formula: C10H10 F2 O2
• Molecular Weight: 200.185
• DSSTox Substance ID: DTXSID30438897
• Wikidata: Q82254739
• Mol file: 144464-70-0.mol

Synonyms:144464-70-0;2,2-difluoro-1-(4-methoxyphenyl)propan-1-one;1-PROPANONE, 2,2-DIFLUORO-1-(4-METHOXYPHENYL)-;1-Propanone, 2,2-difluoro-1-(4-methoxyphenyl)- (9CI);2,2-Difluoro-1-(4-Methoxyphenyl)-1-Propanone;DTXSID30438897;AKOS026749693;F2167-4813

Chemical Property of 1-Propanone, 2,2-difluoro-1-(4-methoxyphenyl)-

Chemical Property:

• PSA: 26.30000
• LogP: 2.53310
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 200.06488588
• Heavy Atom Count: 14
• Complexity: 208

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C(=O)C1=CC=C(C=C1)OC)(F)F

Technology Process of 1-Propanone, 2,2-difluoro-1-(4-methoxyphenyl)-

There total 8 articles about 1-Propanone, 2,2-difluoro-1-(4-methoxyphenyl)- 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: 71.0%

((1-(4-methoxyphenyl)prop-1-en-1-yl)oxy)trimethylsilane → α,α-difluoro-p-methoxypropiophenone (144464-70-0)

Guidance literature:

With N-fluoro-N-(3,5-bis(trifluoromethyl)phenylsulfonyl)benzenesulfonamide; In 1,2-dichloro-ethane; at 50 ℃; for 24h; Inert atmosphere;

DOI:10.1002/chem.202101499

Reference yield: 20.0%

C11H12O4 → α,α-difluoro-p-methoxypropiophenone (144464-70-0)

Guidance literature:

With Selectfluor; In nitromethane; at 60 ℃; for 18h;

DOI:10.1002/adsc.201601315

Reference yield:

ethyl 2,2-difluoropropanoate (28781-85-3) + p-methoxyphenyllithium (14774-77-7) → α,α-difluoro-p-methoxypropiophenone (144464-70-0)

Guidance literature:

In diethyl ether; Ambient temperature;

DOI:10.1016/S0040-4039(00)61141-3

upstream raw materials:

ethyl 2,2-difluoropropanoate

p-methoxyphenyllithium

1-bromo-4-methoxy-benzene

1-(4-methoxyphenyl)ethanone

Downstream raw materials:

methyl 4,4-difluoro-3-(4-methoxyphenyl)-2-pentenoate, (Z)-isomer

methyl 4,4-difluoro-3-(4-methoxyphenyl)-2-pentenoate, (E)-isomer

(Z)-4,4-Difluoro-3-(4-methoxy-phenyl)-pent-2-enoic acid ethyl ester

ethyl (E)-4,4-difluoro-3-(p-methoxyphenyl)pent-2-enoate