N-<2-ethyl>-2-nitro-3-hydroxy-4-methylbenzamide

Base Information

Chemical Name:N-<2-ethyl>-2-nitro-3-hydroxy-4-methylbenzamide
CAS No.:121018-37-9
Molecular Formula:C₁₅H₂₁N₃O₈
Molecular Weight:371.347
Hs Code.:

N-<2-<tris(hydroxymethyl)methylcarbamoyl>ethyl>-2-nitro-3-hydroxy-4-methylbenzamide

Synonyms:

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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 N-<2-ethyl>-2-nitro-3-hydroxy-4-methylbenzamide

Chemical Property:

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Technology Process of N-<2-ethyl>-2-nitro-3-hydroxy-4-methylbenzamide

There total 5 articles about N-<2-ethyl>-2-nitro-3-hydroxy-4-methylbenzamide 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:

: 63115-98-0
6-methylcyclohexa-3a,5-dieno<4,5-d>isoxazoline-3,7-dione N-oxide

: 121018-37-9
N-<2-ethyl>-2-nitro-3-hydroxy-4-methylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dioxane; CHCl₃ / 16 h

2: 85 percent / hydrazine hydrate / ethanol / 16 h

3: hydrochloric acid (15 percent), acetic acid, sodium nitrite / H₂O / 0.25 h

4: H₂O / 15 h / 18 - 20 °C

With hydrogenchloride; hydrazine hydrate; acetic acid; triethylamine; sodium nitrite; In 1,4-dioxane; ethanol; chloroform; water;

Reference yield:

: 6946-15-2
3-hydroxy-4-methyl-2-nitro-benzoic acid

: 121018-37-9
N-<2-ethyl>-2-nitro-3-hydroxy-4-methylbenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: N,N'-dicyclohexylcarbodiimide / dioxane / 0.17 h / 15 °C

2: triethylamine / dioxane; CHCl₃ / 16 h

3: 85 percent / hydrazine hydrate / ethanol / 16 h

4: hydrochloric acid (15 percent), acetic acid, sodium nitrite / H₂O / 0.25 h

5: H₂O / 15 h / 18 - 20 °C

With hydrogenchloride; hydrazine hydrate; acetic acid; triethylamine; dicyclohexyl-carbodiimide; sodium nitrite; In 1,4-dioxane; ethanol; chloroform; water;

Reference yield:

: 121018-27-7
N-(2-ethoxycarbonylethyl)-2-nitro-3-hydroxy-4-methyl-benzamide

: 121018-37-9
N-<2-ethyl>-2-nitro-3-hydroxy-4-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / hydrazine hydrate / ethanol / 16 h

2: hydrochloric acid (15 percent), acetic acid, sodium nitrite / H₂O / 0.25 h

3: H₂O / 15 h / 18 - 20 °C

With hydrogenchloride; hydrazine hydrate; acetic acid; sodium nitrite; In ethanol; water;