N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester

Base Information

Chemical Name:N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester
CAS No.:233266-66-5
Molecular Formula:C₂₂H₁₆F₅NO₂S
Molecular Weight:453.433
Hs Code.:

Synonyms:N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester

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Chemical Property of N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester

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Technology Process of N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester

There total 4 articles about N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester 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: 74.0%

: 5254-86-4
1-mercaptomethylnaphthalene

: methyl ethyl N-pentafluorophenyl-N-allyloxycarbonyl-aminomethyl sulfonium tetrafluoroborate

: 233266-66-5
N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃;
DOI:10.1016/S0040-4020(99)00323-3

Reference yield:

: 771-60-8
2,3,4,5,6-pentafluoroaniline

: 233266-66-5
N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: ethylmagnesium chloride / tetrahydrofuran / 1 h / 20 °C

1.2: 96 percent / tetrahydrofuran / 24 h / 50 °C

2.1: sodium hydride / dimethylformamide

2.2: 2.42 g / dimethylformamide / 2 h / 20 °C

3.1: 76 percent / CH₂Cl₂ / 8 h / 20 °C

4.1: 74 percent / diisopropylethylamine / CH₂Cl₂ / 20 °C

With ethylmagnesium chloride; sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1.1: Metallation / 1.2: Acylation / 2.1: Metallation / 2.2: Alkylation / 3.1: Alkylation / 4.1: Condensation;
DOI:10.1016/S0040-4020(99)00323-3

Reference yield:

: 233266-56-3
N-pentafluorophenyl-carbamic acid allyl ester

: 233266-66-5
N-pentafluorophenyl-N-(1-naphthylmethylthio)methyl-carbamic acid allyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / dimethylformamide

1.2: 2.42 g / dimethylformamide / 2 h / 20 °C

2.1: 76 percent / CH₂Cl₂ / 8 h / 20 °C

3.1: 74 percent / diisopropylethylamine / CH₂Cl₂ / 20 °C

With sodium hydride; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; 1.1: Metallation / 1.2: Alkylation / 2.1: Alkylation / 3.1: Condensation;
DOI:10.1016/S0040-4020(99)00323-3