HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 69527272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trimethylphosphine | HCID 68983 | — |
| Reactant | (1-Bromoprop-2-en-1-yl)benzene | HCID 15361356 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 69527272 | HCID 69527272 | 82.2% |
Reaction Steps
Trimethylphosphine (50.0 ml of a 1.0 molar solution in tetrahydrofuran, 5.00×10−2 mol) was added via addition funnel over about 2 minutes into a thoroughly nitrogen degassed dispersion of vinylbenzyl bromide (9.85 g, 5.00×10−2 mol) in diethyl ether (100 ml). A solid precipitate began to form almost immediately. The reaction was allowed to stir for 4 hours at room temperature, then was placed in a freezer overnight. The solid product was isolated by filtration, washed three times with 100 ml of diethyl ether, and dried under vacuum for 2 hours. Pure product (11.22 g) was recovered as a white powder (82.20% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06537730B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-563e094d942347f9aae646ff93b45f44 |
| Source note | uspto-grants-2003_03 |