Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358691Generated: November 2, 2026

Methylamine → HCID 15482079, compound

https://huagongshe.com/reaction/1358691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium HydroxideHCID 14798—
Reactant2,4,6-Cycloheptatriene-1-carbonitrileHCID 139516—
SolventMethanolHCID 887—
ProductHCID 15482079HCID 1548207970%

Reaction Conditions

Temperature125 °C

Reaction Steps

In 2 ml of methanol was dissolved 0.5 g (4.27 mmol) of 2,4,6-cycloheptatriene-1-carbonitrile (4: CHT-CN). A solution of 171 mg (4.27 mmol) of sodium hydroxide in 5 ml of methanol and then 3 ml (about 38 mmol) of 40% methanolic solution of methylamine were added thereto, and the resulting mixture was stirred with heating at 125° C. for 10 hours in a sealed vessel. After standing at room temperature, the methanol was evaporated and the residue was adjusted to pH 2 with 1N sulfuric acid solution, followed by extraction with chloroform (No. of run: 1) or ether (No. of run: 2 to 5) (separation into an organic layer 1 and an aqueous layer 1). The aqueous layer 1 was neutralized with 4N sodium hydroxide solution, followed by extraction with chloroform (No. of run: 1) or ether (No. of run: 2 to 5) (separation into an organic layer 2 and an aqueous layer 2). The organic layer 2 was dried and then the solvent was evaporated therefrom to obtain 0.458 g of a brown oil (1RS)-AECG-CN (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596868B2
Source datasetuspto-grants-2003_07
ORD IDord-d8faa37e93234cbe973607bd5eb3c6e8
Source noteuspto-grants-2003_07