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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500541Generated: November 3, 2026

Methyl isothiocyanate → HCID 178481696, compound

https://huagongshe.com/reaction/500541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl isothiocyanateHCID 11167—
Reactant2-Oxo-1-(2-trimethylsilanyl-ethoxymethyl)-1,2-dihydro-pyridine-4-carboxylic acid hydrazideHCID 68458824—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178481696HCID 178481696105.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

The title compound of Example 20.1 (19.0 g, 67.0 mmol) was stirred in methanol (150 mL) and heated to 60° C. Methyl isothiocyanate (5.04 mL, 73.7 mmol) was then added via a syringe. After stirring for 40 minutes, a solution on NaOH (2.95 g, 73.7 mmol) in water (30 mL) was added and the reaction mixture was stirred at 60° C. overnight. The reaction mixture was cooled to room temperature and concentrated. The aqueous residue was neutralized, extracted with chloroform, and the organic layer dried over sodium sulfate and concentrated. The residue was purified by silica gel using ethyl acetate to give the product (24.0 g, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772235B2
Source datasetuspto-grants-2010_08
ORD IDord-551fe588aac344159b1086df724037fe
Source noteuspto-grants-2010_08