HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4,4'-Dipentyl-4-prop-1-ynylbicyclohexyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Reactant | 4-Ethynyl-4,4'-dipentylbicyclohexyl | HCID 15451976 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4,4'-Dipentyl-4-prop-1-ynylbicyclohexyl | HCID 15451977 | — |
Reaction Steps
9.66 ml of a 15% solution of n-butyllithium in hexane are added dropwise at −70° C. to 4.80 g of 4-ethynyl-4,4′-dipentylbicyclohexyl in 40 ml of THF, and the mixture is stirred for 15 minutes. A solution of 0.99 ml of iodomethane and 1.914 ml of 1,3-dimethyltetrahydro-2-pyrimidinone in 10 ml of THF is subsequently added dropwise to the reaction solution at this temperature, and the cooling is removed. Conventional work-up gives 4,4′-dipentyl-4-prop-1-ynylbicyclohexyl (C 35 N 35.4 I, Δε−1.54, Δn 0.01).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06303194B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-b0135a888f6647fa960c31c4515352b0 |
| Source note | uspto-grants-2001_10 |