dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid

Base Information

Chemical Name:dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid
CAS No.:137180-81-5
Molecular Formula:C₁₆H₁₈NO₄P
Molecular Weight:319.297
Hs Code.:

Synonyms:dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid

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Chemical Property of dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid

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Technology Process of dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid

There total 3 articles about dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid 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: 87.0%

: 538-51-2
benzylidene phenylamine

: 149-73-5
trimethyl orthoformate

: 26624-91-9
dimethyl (phenyl)(phenylamino)methylphosphonate

: 137180-81-5
dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid

Guidance literature:: With phosphorus trichloride; In dichloromethane; for 0.5h;
DOI:10.1080/00397919108021787

Reference yield: 85.0%

: 26624-91-9
dimethyl (phenyl)(phenylamino)methylphosphonate

: 149-73-5
trimethyl orthoformate

: 137180-81-5
dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid

Guidance literature:: With hydrogenchloride; In toluene; for 5h; Heating;
DOI:10.1080/00397919108021787

Reference yield:

: 538-51-2
benzylidene phenylamine

: 137180-81-5
dimethyl ester of 1-phenyl N-formyl-N-phenylaminomethanephosphonic acid

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 1 h / Heating

2: 85 percent / HCl / toluene / 5 h / Heating

With hydrogenchloride; In toluene;
DOI:10.1080/00397919108021787