Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051242Generated: November 1, 2026

Methyl Isocyanate → HCID 54306683, compound

https://huagongshe.com/reaction/2051242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
ReactantHCID 53857608HCID 53857608—
SolventWaterHCID 962—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 54306683HCID 5430668338.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl isocyanate (0.33 g, 5.8 mmol) is added dropwise to 2-[[3-(N-hydroxyamino)methyl-2-methylphenyl]amino]benzoic acid methyl ester (1.5 g, 5.2 mmol) in 33% water/dioxane (60 mL) with ice bath cooling. The reaction mixture is stirred at 0° C. for 30 minutes and then at room temperature for 1 hour. It is then diluted with water (100 mL) and extracted with ethyl acetate (200 mL). The organic layer is washed with water (50 mL) and dried over magnesium sulfate. Evaporation of the ethyl acetate gives the crude product which is purified by recrystallization first from ether and then from ethyl acetate to give 2-[[3-[[hydroxy[(methylamino)carbonyl]amino]methyl]2-methylphenyl]amino]benzoic acid methyl ester (0.68 g, 38%). mp=173-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017604
Source datasetuspto-grants-1991_05
ORD IDord-81468cd5bacc49af95eaf918dc4bff84
Source noteuspto-grants-1991_05