HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Cyclopentylbenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclopentene | HCID 8882 | — |
| Reactant | 3-Iodobenzyl alcohol | HCID 42300 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Cyclopentylbenzyl alcohol | HCID 53788593 | 232.3% |
Reaction Steps
According to example 61, 10.0 g of 3-iodobenzyl alcohol (Aldrich) was treated with 30 mL of cyclopentene using 0.96 g of Pd(OAc)2, 2.60 g of tri-ortho-tolylphosphine, and 6.6 mL of Et3N. The resulting olefin mixture was hydrogenated for 2.5 h using 0.62 g of 5% Pt(C) in MeOH to afford 5.77 g (76%) of 3-cyclopentylbenzyl alcohol as a light yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06319702B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-b8be302024d646a387679770a18ecb4b |
| Source note | uspto-grants-2001_11 |