N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide

Base Information

Chemical Name:N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide
CAS No.:116911-53-6
Molecular Formula:C₁₂H₁₅N₃O₆S
Molecular Weight:329.334
Hs Code.:

Synonyms:N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide

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Chemical Property of N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide

Chemical Property:

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Technology Process of N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide

There total 7 articles about N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide 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:

: 106994-14-3
N-<4-acetamido-5-(benzyloxy)-2-nitrophenyl>-N-(2-propenyl)methanesulfonamide

: 116911-53-6
N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide

Guidance literature:: With boron tribromide;
DOI:10.1016/S0040-4039(00)84617-1

Reference yield:

: 25351-89-7
N-(2-hydroxy-4-nitrophenyl)acetamide

: 116911-53-6
N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1: 84 percent / KI, K₂CO₃ / dimethylformamide / 4 h

2: Zn, CaCl₂, ethanol / 1.5 h / Heating

3: 80 percent / pyridine / CH₂Cl₂ / 2 h / 25 °C

4: 74 percent / HNO₃, mercuric acetate, acetic anhydride / acetic acid / 0.75 h / 0 °C

5: 76 percent / potassium tert-butoxide / dimethylformamide / 4 h / 25 °C

6: BBr₃, cyclohexane / CH₂Cl₂; ethanol / 0.5 h / -20 °C

With pyridine; ethanol; cyclohexane; potassium tert-butylate; mercury(II) diacetate; nitric acid; acetic anhydride; boron tribromide; potassium carbonate; potassium iodide; calcium chloride; zinc; In ethanol; dichloromethane; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jo00256a036

Reference yield:

: 25945-95-3
N-<2-(benzyloxy)-4-nitrophenyl>acetamide

: 116911-53-6
N-(4-acetamido-5-hydroxy-2-nitrophenyl)-N-(2-propenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: Zn, CaCl₂, ethanol / 1.5 h / Heating

2: 80 percent / pyridine / CH₂Cl₂ / 2 h / 25 °C

3: 74 percent / HNO₃, mercuric acetate, acetic anhydride / acetic acid / 0.75 h / 0 °C

4: 76 percent / potassium tert-butoxide / dimethylformamide / 4 h / 25 °C

5: BBr₃, cyclohexane / CH₂Cl₂; ethanol / 0.5 h / -20 °C

With pyridine; ethanol; cyclohexane; potassium tert-butylate; mercury(II) diacetate; nitric acid; acetic anhydride; boron tribromide; calcium chloride; zinc; In ethanol; dichloromethane; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jo00256a036