4,4'-dimethoxybenzhydryl fluoroacetate

Base Information Edit

Chemical Name:4,4'-dimethoxybenzhydryl fluoroacetate
CAS No.:1580541-38-3
Molecular Formula:C₁₇H₁₇FO₄
Molecular Weight:304.318
Hs Code.:
Mol file:1580541-38-3.mol

Synonyms:4,4'-dimethoxybenzhydryl fluoroacetate

Suppliers and Price of 4,4'-dimethoxybenzhydryl fluoroacetate

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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 4,4'-dimethoxybenzhydryl fluoroacetate Edit

Chemical Property:

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Technology Process of 4,4'-dimethoxybenzhydryl fluoroacetate

There total 2 articles about 4,4'-dimethoxybenzhydryl fluoroacetate 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: 64.5%

: 359-06-8
monofluoroacetyl chloride

: 728-87-0
4,4'-Dimethoxybenzhydrol

: 1580541-38-3
4,4'-dimethoxybenzhydryl fluoroacetate

Guidance literature:: With pyridine; In benzene; at 20 ℃; for 12h; Inert atmosphere;
DOI:10.1002/ejoc.201301574 DOI:10.1002/ejoc.201301574

Reference yield:

: 90-96-0
bis(p-methoxyphenyl)methanone

: 1580541-38-3
4,4'-dimethoxybenzhydryl fluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate / methanol

2: pyridine / benzene / 12 h / 20 °C / Inert atmosphere

With pyridine; sodium tetrahydroborate; In methanol; benzene;
DOI:10.1002/ejoc.201301574

Reference yield:

: 1580541-38-3
4,4'-dimethoxybenzhydryl fluoroacetate

: 144-49-0
Fluoroacetic acid

: 728-87-0
4,4'-Dimethoxybenzhydrol

Guidance literature:: With water; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; In dichloromethane; acetonitrile; at 25 ℃; Solvent; Reagent/catalyst; Kinetics; Solvolysis;
DOI:10.5562/cca2495