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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432059Generated: October 31, 2026

Methanol → N-methyl-2-(2-hydroxyphenyl)-2-methoxyiminoacetamide

https://huagongshe.com/reaction/432059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethylamineHCID 6329—
Reactantmethyl E-2-(2-hydroxyphenyl)-2-methoxyimino-acetateHCID 135424589—
ReactantHCID 136127060HCID 136127060—
SolventTetrahydrofuranHCID 8028—
ProductN-methyl-2-(2-hydroxyphenyl)-2-methoxyiminoacetamideHCID 136045378—

Reaction Conditions

Temperature10 °C

Reaction Steps

0.5 g (0.0013 mol) of methyl 2-(2-hydroxyphenyl)-2-methoxyimino-acetate (in particular Example II-Id from process step 4; HPLC: 54.4% methyl Z-2-(2-hydroxyphenyl)-2-methoxyimino-acetate of log p=2.39 is disolved in 6 ml of tetrahydrofuran and cooled to 10° C. With cooling, methylamine is introduced. After about 30 minutes, 2 ml of methanol are added, the solution is saturated with methylamine and the mixture is allowed to stand at 10° C. overnight. The solvents are distilled off under reduced pressure and the residue is mixed with a mixture of 5 ml of 2 N hydrochloric acid and 5 ml of saturated sodium chloride solution and extracted three times with 10 ml of ethyl acetate each time. The organic phase is dried over sodium sulphate and the solvent is distilled off under reduced pressure, giving 0.6 g of crude product. This crude product is chromatographed with a mixture of 7 parts of n-hexane and 3 parts of acetone on silica gel. This gives 0.4 g of product which, according to HPLC, contains 99.2% N-methyl-Z-2-(2-hydroxyphenyl)-2-methoxyiminoacetamide of log p=1.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660872B1
Source datasetuspto-grants-2003_12
ORD IDord-82ee7253664048e88ba1ff2cea2b10f6
Source noteuspto-grants-2003_12