HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77416Generated: October 30, 2026
Methyl iodide → (4-Methyloxan-4-yl)methanamine
https://huagongshe.com/reaction/77416
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Oxane-4-carbonitrile | HCID 11815837 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Methyloxan-4-yl)methanamine | HCID 54165201 | — |
Reaction Steps
A mixture of tetrahydropyran-4-carbonitrile (5.00 g) and THF (50 ml) was admixed at 0° C. with lithium hexamethyldisilazide (1 M, 63 ml), and, after 90 minutes, methyl iodide (4.26 ml) was added dropwise with good cooling. After 12 hours, the reaction mixture was partitioned between water and ethyl acetate. The organic phase was dried over sodium sulfate and concentrated. The residue was dissolved in THF (200 ml), and lithium aluminum hydride (3.79 g) was added. The mixture was boiled at reflux for 6 hours, Water (3.8 ml) and then sodium hydroxide solution (40%; 3.8 ml) were cautiously added dropwise to the cooled suspension. The precipitate was filtered off and the filtrate was concentrated. This afforded the product with the molecular weight of 129.20 (C7H15NO); MS (ESI): 130 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08841290B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-a2bd06b7db1b40bd8dce4a86a9d426f5 |
|---|
| Source note | uspto-grants-2014_09 |
|---|