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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864320Generated: October 30, 2026

HCID 86749903, compound → HCID 145828514, compound

https://huagongshe.com/reaction/864320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86749903HCID 86749903—
ReactantHCID 145828517HCID 145828517—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
ProductHCID 145828514HCID 145828514—

Reaction Steps

Methyl (E)-3-amino-alpha-hydroxyiminophenylacetate can be obtained in the following manner: the reaction is carried out as in Example 9 for the preparation of ethyl (Z)-3-amino-alpha-tert-butoxycarbonylmethoxyimino-phenylacetate, but starting from 3.4 g of methyl (E)-3-nitro-alpha-hydroxyiminophenylacetate and 0.034 g of platinum dioxide in 20 cm3 of methanol. After treatment, 2.9 g of methyl (E)-3-amino-alpha-hydroxyiminophenylacetate are obtained in the form of a solid which is used as such in the subsequent syntheses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563136
Source datasetuspto-grants-1996_10
ORD IDord-6092071ac0874e249955b547a83ac3bd
Source noteuspto-grants-1996_10