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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791104Generated: November 2, 2026

Methyl iodide → HCID 22027369, compound

https://huagongshe.com/reaction/1791104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
Reactant5-Bromo-2,3-dichloropyridineHCID 12747760—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22027369HCID 2202736927.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under nitrogen, 4.1 g of the title compound from Step B was added to a suspension of sodium hydride (60% oil suspension) in 30 mL of dry N,N-dimethylformamide, cooled to 0° C. N-(Diphenylmethylene)glycine ethyl ester (4.6 g) was added in portions with no exotherm, and the mixture was stirred at room temperature for 3 hours. Then, 3.4 mL of methyl iodide was added at <30° C. and the reaction mixture was stirred overnight at room temperature. The reaction mixture was diluted with water and extracted with diethyl ether (2×). The combined extracts were washed with saturated brine (1×) and reduced in vacuo to an oil that was then refluxed in 50 mL of 12N HCl for 4 hours. The reaction mixture was reduced in vacuo to an oil, cooled, and slurried with diethyl ether overnight. The ether was then decanted off and the residue was dried in a vacuum oven to give 1.3 g of the desired intermediate as a solid. NMR(CDCl3; 300 MHz): 1.40 and 1.46 (2 doublets, 3H, J is 7.0 Hz), 4.7 (m, 1H), 8.48 (d, 1H, J is 1.8), 8.6 (bs, 3H), 8.79 (d, 1H, J is 1.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074742B2
Source datasetuspto-grants-2006_07
ORD IDord-6a4dd3eb78ac4e96a9746bc45aadf081
Source noteuspto-grants-2006_07