4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one

Base Information

Chemical Name:4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one
CAS No.:1312297-21-4
Molecular Formula:C₁₆H₁₂N₂O₅
Molecular Weight:312.282
Hs Code.:

Synonyms:4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one

Suppliers and Price of 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one

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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 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one

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Technology Process of 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one

There total 2 articles about 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one 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: 52.0%

: 71917-43-6
2-Hydroxy-2-(2-hydroxy-5-methoxy-phenyl)-indan-1,3-dione

: 1312297-21-4
4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one

Guidance literature:: With hydroxylamine hydrochloride; In ethanol; for 3h; Reflux;
DOI:10.1016/j.tetlet.2011.04.076

Reference yield:

: 485-47-2
indan-1,2,3-trione hydrate

: 150-76-5
4-methoxy-phenol

: 1312297-21-4
4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / Reflux

2: hydroxylamine hydrochloride / ethanol / 3 h / Reflux

With hydroxylamine hydrochloride; acetic acid; In ethanol;
DOI:10.1016/j.tetlet.2011.04.076