HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 23212442, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Product | HCID 23212442 | HCID 23212442 | — |
Reaction Steps
4-Bromobenzylalcohol(5.0 g, 26.7 mmol) was dissolved in THF (130 ml) and methyl iodide added (6.7 ml, 107.0 mmol). Sodium hydride (1.20 g of 80% dispersion in oil, 40.1 mmol) was added in two portions while stirring at room temperature under nitrogen. After stirring for 2 hours, the solvents were removed in vacuo and the residue partitioned between water and ether. The water was reextracted with ether and the combined organic fractions were then washed with water and brine before drying (Na2SO4) and evaporating in vacuo to give 4-bromobenzylmethyl ether as an orange liquid (5.3 g, 26.4 mmol). δH (250 MHz, CDCl3) 3.39 (3H, s, CH3), 4.40 (2H, s, CH2), 7.21 (2H, d, J 7.5 Hz, Ar--H), 7.48 (2H, d, J 7.5 Hz, Ar--H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05559125 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-8f76bb48152a4900a121ee30cbfc5e0a |
| Source note | uspto-grants-1996_09 |