HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-Bromomethyl-6-fluoro-3-pentylchroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | (6-Fluoro-3-pentylchroman-7-yl)methanol | HCID 59288346 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Bromomethyl-6-fluoro-3-pentylchroman | HCID 59288330 | — |
Reaction Steps
10.2 g (38.9 mmol) of triphenylphosphine are suspended in 80 ml of acetonitrile, and 2.0 ml (39.0 mmol) of bromine are added dropwise with ice cooling. A solution of 10.0 g (38.4 mmol) of (6-fluoro-3-pentylchroman-7-yl)methanol in 20 ml of acetonitrile is subsequently added, and the mixture is stirred overnight at room temp. After addition of water, the mixture is extracted three times with n-heptane, and the combined org. phases are washed with water and dried over sodium sulfate. The solvent is removed in vacuo, and the residue is filtered through silica gel with heptane/toluene (4:1), giving 7-bromomethyl-6-fluoro-3-pentylchroman as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07955664B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-abd18b9303804278a968543070d90dab |
| Source note | uspto-grants-2011_06 |