ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride

Base Information

Chemical Name:ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride
CAS No.:82128-80-1
Molecular Formula:C₁₁H₁₄ClNO₃*ClH
Molecular Weight:280.151
Hs Code.:

Synonyms:ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride

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Chemical Property of ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride

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Technology Process of ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride

There total 3 articles about ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride 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: 91.0%

: 64-17-5
ethanol

: 82128-79-8
2-(5-chloro-2-methoxyphenyl)-2-trimethylsiloxyethanenitrile

: 82128-80-1
ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride

Guidance literature:: With hydrogenchloride; at 5 ℃; for 16h;
DOI:10.1021/jm00155a030

Reference yield: 91.0%

: 82128-18-5
5-chloro-2-methoxybenzaldehyde cyanohydrin

: ethyl 1-(5-Chloro-2-methoxy)-1-hydroxymethanecarboximidate

: 82128-80-1
ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride

Guidance literature:

Reference yield:

: 7035-09-8
5-chloro-2-methoxybenzaldehyde

: 82128-80-1
ethyl 1-(5-chloro-2-methoxyphenyl)-1-hydroxymethanecarboximidate hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: ZnI₂ / CH₂Cl₂ / 65 h / Ambient temperature

2: 91 percent / HCl / 16 h / 5 °C

With hydrogenchloride; zinc(II) iodide; In dichloromethane;
DOI:10.1021/jm00155a030