ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate

Base Information

Chemical Name:ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate
CAS No.:131292-08-5
Molecular Formula:C₃₂H₂₇O₄P
Molecular Weight:506.538
Hs Code.:

Synonyms:ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate

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Chemical Property of ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate

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Technology Process of ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate

There total 3 articles about ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate 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: 66.0%

: 62848-99-1
(2-methoxy-phenyl)-propioloyl chloride

: 1099-45-2
ethyl (triphenylphosphoranylidene)acetate

: 131292-08-5
ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate

Guidance literature:: With triethylamine; In toluene; for 3h; Ambient temperature;
DOI:10.1039/P19940002461

Reference yield:

: 7342-00-9
3-(2-methoxyphenyl)prop-2-ynoic acid

: 131292-08-5
ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) aq. NaOH, 2.) SOCl₂ / 2) ether, reflux, 6 h

2: 66 percent / Et₃N / toluene / 3 h / Ambient temperature

With sodium hydroxide; thionyl chloride; triethylamine; In toluene;
DOI:10.1039/P19940002461

Reference yield:

: 80220-94-6
ethyl 3-(2-methoxyphenyl)prop-2-ynoate

: 131292-08-5
ethyl 5-(2-methoxyphenyl)-3-oxo-2-triphenylphosphoranylidenepent-4-ynoate

Guidance literature:: Multi-step reaction with 3 steps

1: NaOH, benzyltriethylammonium chloride / H₂O; diethyl ether / 120 h

2: 1.) aq. NaOH, 2.) SOCl₂ / 2) ether, reflux, 6 h

3: 66 percent / Et₃N / toluene / 3 h / Ambient temperature

With sodium hydroxide; thionyl chloride; N-benzyl-N,N,N-triethylammonium chloride; triethylamine; In diethyl ether; water; toluene;
DOI:10.1039/P19940002461