HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 10494674, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 6-Isopropylquinoline | HCID 67285 | — |
| Reactant | HCID 178440986 | HCID 178440986 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10494674 | HCID 10494674 | 40.6% |
Reaction Steps
To a cooled (ice bath) 2M diethyl ether solution of 4-tert-butylphenylmagnesium bromide (15 ml, 0.03 mol) was added dropwise under argon 15 ml of a tetrahydrofuran solution of 6-isopropylquinoline (5.13 g, 0.03 mol). The resulting mixture was refluxed for 5 hours, stirred at room temperature for 12 hours and quenched with water (80 ml). The yellow precipitate obtained was then filtered and washed with hexane. Crystallization in hexane:chloroform 40:1 yielded 3.7 g of pure (+)-2-(4-tert-butylphenyl)-6-isopropylquinoline (40% yield). 1H NMR(CDCl3): 8.2 (m, ArH, 4H), 7.84 (m, ArH, 1H), 7.60 (m, ArH, 4H), 3.12 (s, CH(Me)2, 1H), 1.4 (s, CH(Me)2 and C(Me)3, 15H); Mass/Cl—NH3: MH− 304.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06770668B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-774d378659fb4d4da242dfc635273e37 |
| Source note | uspto-grants-2004_08 |