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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227710Generated: October 30, 2026

Methyl iodide → HCID 67455812, compound

https://huagongshe.com/reaction/227710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10636289HCID 10636289—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67455812HCID 6745581241%

Reaction Conditions

Temperature0 °C

Reaction Steps

Iodomethane (0.314 mL, 5.04 mmol, 1.1 equiv) and sodium hydride (60% in mineral oil, 202 mg, 5.04 mmol, 1.1 equiv) were combined in DMF (10 mL) and cooled to 0° C. The product of Step (b) (1.275 g, 4.59 mmol, 1 equiv) was added slowly as a solution in DMF (11 mL). Following the addition, the reaction was warmed to room temperature and stirred for two hours. The reaction mixture was diluted with water and poured into EtOAc. The phases were separated and the aqueous phase was extracted with an additional portion of EtOAc. The combined organic phases were washed with water, 15% aq. Na2S2O4, and satd. NaCl, then dried over sodium sulfate. The suspension was filtered and the filtrate was concentrated en vacuo to afford a mixture of two regioisomeric products. The isomers were separated by flash chromatography (3→5% Et2O/CH2Cl2), and regiochemistry of the desired product was confirmed by NOE analysis. 550 mg (41%) of the title compound was isolated as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.30-7.27 (m, 2H), 7.02-6.97 (m, 2H), 5.21 (s, 1H), 3.91 (s, 3H), 3.63 (s, 3H), 2.84 (s, 3H), 2.38 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560467B2
Source datasetuspto-grants-2009_07
ORD IDord-4342352c23f8412fbbe92af813cf9500
Source noteuspto-grants-2009_07