Abstract
2-Bromo-3-methoxy-1,3-dimethylcyclopentene (3). is synthesized in 85% yield in 80 g scale by 1,2-addition of MeLi to 2-bromo-3-methyl-2-cyclopenten-1-one and subsequent in situ treatment of MeI. Addition of n-BuLi to the bromo-compound 3 in Et2O affords 2-lithio-3-methoxy-1,3- dimethylcyclopentene (1). Successive addition of RCHO [R = CH3, (CH2)2CH3, CH(CH3)2, C(CH3)3, H] and MeI to the lithium compound and aqueous acidic work-up provide cyclopentadiene compounds, 2-[CHR(OMe)]-1,3-Me 2C5H3 in 60-84% yields. Treatment of the cyclopentadienes with NaH or KH in pentane affords 1,4,6-trimethylfulvene, 6-n-propyl-1,4-dimethylfulvene, 6-isopropyl-1,4-dimethylfulvene, 6-tert-butyl-1,4-dimethylfulvene and 1,4-dimethylfulvenein 67-83% yields. Ligand for an ansa-metallocene complex, CH2C(1,3-Me2Cp) 2ZrCl2, can be shortly afforded in 64% yield by reacting the lithium compound 1 with the newly synthesized 1,4-dimethylfulvene.
| Original language | English |
|---|---|
| Pages (from-to) | 1052-1056 |
| Number of pages | 5 |
| Journal | Synthesis |
| Issue number | 7 |
| DOIs | |
| State | Published - 6 May 2004 |
Keywords
- Cyclopentadienes
- Fulvene synthesis
- Lithiation
- Metallocenes
- Organometallic reagents
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