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Azane;hydrate → O-(4-cyano-2-ethoxybenzyloxy)hydroxyamine

HRID 1294452
Notes
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Reaction equation

HRID 1294452 reaction equation
Cl.[C:2]([C:4]1[CH:12]=[CH:11][C:7]([CH2:8][O:9]N)=[C:6]([O:13][CH2:14][CH3:15])[CH:5]=1)#[N:3].[OH2:16].[NH3:17]>>[C:2]([C:4]1[CH:12]=[CH:11][C:7]([CH2:8][O:9][O:16][NH2:17])=[C:6]([O:13][CH2:14][CH3:15])[CH:5]=1)#[N:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 12896473Azane;hydrateHCID 69434226O-(4-cyano-2-ethoxybenzyl)hydroxyamine hydrochloride

Product 1

HCID 86609490O-(4-cyano-2-ethoxybenzyloxy)hydroxyamine

Procedure

The O-(4-cyano-2-ethoxybenzyl)hydroxyamine hydrochloride (19) and ammonia water were mixed, then, extracted with ethyl acetate to obtain O-(4-cyano-2-ethoxybenzyl)hydroxyamine (18) (80 mg, 0.42 mmol). This was dissolved in acetonitrile (12 ml), then, several drops of 85% phosphoric acid aqueous solution were dropped on this, and the produced white solid was filtrated by filtration under reduced pressure. The filtrated substance was washed with acetonitrile, then, the filtrated substance was recovered and dried by a vacuum pump to obtain 60 mg of a while solid.

Workup

  1. extractionextracted with ethyl acetate

Sources & evidence

ORD record
ord-b8ac6282859a4fbf923ef2bb1378f113
Source dataset
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07241625B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes