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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442642Generated: November 2, 2026

Methyl iodide → HCID 58612179, compound

https://huagongshe.com/reaction/1442642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 26580537HCID 26580537—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58612179HCID 58612179—

Reaction Steps

Methyl iodide (0.728 mL, 11.7 mmol) was added to (4-nitro-benzyl)-[(2R)-tetrahydro-furan-2-ylmethyl]-amine Compound 10a2 (1.84 g, 7.80 mmol) and potassium carbonate (3.23 g, 23.4 mmol) in DMF (30 mL). After 4 hrs the reaction was diluted with water and extracted with ethyl ether. The combined extracts were washed with water, dried over MgSO4, and evaporated down to give 1.43 g of methyl-(4-nitro-benzyl)-[(2R)-tetrahydro-furan-2-ylmethyl]-amine Compound 10a3. Using the procedure of Example 21, Compound 10a3 was used in place of Compound 21a2 and carried forward to prepare 4-({methyl-[(2R)-tetrahydro-furan-2-ylmethyl]-amino}-methyl)-phenylamine Compound 10a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659284B2
Source datasetuspto-grants-2010_02
ORD IDord-ebadefbcbd634f22a6d67834cab1e080
Source noteuspto-grants-2010_02