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3'-chloro-2'-methoxy-5'-methylisonitrosoacetanilide

Base Information
  • Chemical Name:3'-chloro-2'-methoxy-5'-methylisonitrosoacetanilide
  • CAS No.:253268-32-5
  • Molecular Formula:C10H11ClN2O3
  • Molecular Weight:242.662
  • Hs Code.:
3'-chloro-2'-methoxy-5'-methylisonitrosoacetanilide

Synonyms:3'-chloro-2'-methoxy-5'-methylisonitrosoacetanilide

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Chemical Property of 3'-chloro-2'-methoxy-5'-methylisonitrosoacetanilide
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Technology Process of 3'-chloro-2'-methoxy-5'-methylisonitrosoacetanilide

There total 1 articles about 3'-chloro-2'-methoxy-5'-methylisonitrosoacetanilide 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:
Guidance literature:
chloral hydrate; 3-chloro-2-methoxy-5-methylaniline; With hydrogenchloride; sodium sulfate; In water; N,N-dimethyl-formamide; at 90 ℃; for 0.416667h;
With hydroxylamine hydrochloride; In water; N,N-dimethyl-formamide; at 90 ℃; for 18h;
DOI:10.1016/S0223-5234(99)00220-2
Guidance literature:
Multi-step reaction with 2 steps
1: 82 percent / polyphosphoric acid / 3 h / 80 °C
2: 70 percent / aq. NaOH; 30 percent H2O2 / dioxane / 3 h / 5 - 20 °C
With sodium hydroxide; PPA; dihydrogen peroxide; In 1,4-dioxane; 1: Cyclization / 2: Ring cleavage;
DOI:10.1016/S0223-5234(99)00220-2
Guidance literature:
Multi-step reaction with 3 steps
1.1: 82 percent / polyphosphoric acid / 3 h / 80 °C
2.1: 70 percent / aq. NaOH; 30 percent H2O2 / dioxane / 3 h / 5 - 20 °C
3.1: HCl / diethyl ether
3.2: 47 percent / BBr3 / CH2Cl2 / 43 h / -65 - 20 °C
With hydrogenchloride; sodium hydroxide; PPA; dihydrogen peroxide; In 1,4-dioxane; diethyl ether; 1.1: Cyclization / 2.1: Ring cleavage / 3.1: Addition / 3.2: demethylation;
DOI:10.1016/S0223-5234(99)00220-2
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