HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromopentane → HCID 15122333, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (Furan-2-yl)(phenyl)methanol | HCID 3746348 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Product | HCID 15122333 | HCID 15122333 | — |
Reaction Steps
9 grams of the distilled 1-furyl-1-phenyl-methanol (0.052 mole) is charged to a reactor with 0.39 g (2 mole percent) tetrabutylammonium iodide and 10.4 g of a 50 percent aqueous solution of sodium hydroxide added over a 10 minute period with stirring. This is followed by addition of 17.6 g (0.14 mole) 1-bromopentane over a period of 10 minutes and the reaction mixture allowed to stir for 2 hours. The reaction mixture is then extracted with diethyl ether which, after drying over magnesium sulfate, is evaporated. The resulting crude product is short-path distilled to obtain 2-(methoxy, phenylmethyl)furan in low yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536349 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-5fe7c36c7dab4d1d8f9e720c48df498d |
| Source note | uspto-grants-1985_08 |