HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 2-(Allyloxymethyl)-1-fluoro-3-iodobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (2-Fluoro-6-iodophenyl)methanol | HCID 59705003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Allyloxymethyl)-1-fluoro-3-iodobenzene | HCID 59705016 | — |
Reaction Steps
To a solution of (2-fluoro-6-iodophenyl)methanol (10 mmol) in 50 mL of THF was added NaH (12 mmol) in small portions at room temperature. After the addition, allylbromide (12 mmol) was added slowly via syringe. The reaction mixture was stirred 16 hours at room temperature. The resulting white heterogeneous mixture was quenched with water and then diluted with 100 mL of Et2O, followed by washing with water and brine. The organic layer was dried over MgSO4 and then concentrated to dryness in vacuo to offer 2.8 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915268B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-ba745505ca6949139ce0920bfd1a7550 |
| Source note | uspto-grants-2011_03 |