HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585468Generated: October 25, 2026
Methanol → (3-Methoxy-2-methylpropyl)benzene
https://huagongshe.com/reaction/1585468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Methyl-3-phenyl-1-propanol | HCID 95640 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3-Methoxy-2-methylpropyl)benzene | HCID 22336876 | — |
Reaction Steps
220 ml (1.9 mole) of KH (35% in oil) were placed, under a N2 -atmosphere, into a 4.5 l reactor and washed 4 times with pentane, in order to remove all traces of oil. 1.5 l of dry tetrahydrofurane were added before the dropwise addition of a solution of 259 g (1.73 mole) of 1-hydroxy-2-methyl-3-phenylpropane and 500 ml of dry tetrahydrofurane. The reaction was stirred for 15 hours at room temperature. Then 285 g (2.01 mole) of methyl iodide were added dropwise over a period of 2 hours, and stirring was continued at room temperature for another 2 hours. A possible excess of KH was hydrolyzed by adding 50 ml of methanol, then the reaction mixture was poured on ice. The product was taken up in ether, which was washed 3 times with a saturated NH4Cl solution and then with brine to neutrality. After drying over Na2SO4, the solution was filtered, concentrated and then distilled over a Vigreux-type column (boiling point: 100° C. at 5×102Pa).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05939368 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-9389ecb1ff064e058e58d000cafba1be |
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| Source note | uspto-grants-1999_08 |
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