HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778455Generated: November 1, 2026
HCID 22023067, compound → HCID 131734810, compound
https://huagongshe.com/reaction/1778455
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22023067 | HCID 22023067 | — |
| Reactant | HCID 86724410 | HCID 86724410 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 131734810 | HCID 131734810 | — |
Reaction Steps
To a green solution of dimethyl(2,3,4,5-tetramethylcyclopenta-2,4-dien-1-yl)silyl trifluoromethanesulfonate (7.50 g, 22.8 mmol, 1.00 eq.) in ether (25 mL) at −35° C. was added lithium (2-ethyl-4-phenylindenide) (5.53 g, 24.4 mmol, 1.07 equiv.) in portions to give a hazy yellow solution near room temperature. The reaction was stirred for 20 hours, then evaporated under vacuum, leaving a light yellow semi-solid. The residue was extracted with pentane (3×40 mL) and the extract was filtered to give a yellow solution and pale yellow-white solid. The solution was evaporated under vacuum to yield thick, yellow oil. Yield 9.28 g (102%). 1H NMR(C6D6): δ 7.64 (d, 2H), 7.43 (d, 1H), 7.35 (d, 1H), 7.29 (t, 2H), 7.19 (t, 2H), 6.95 (s, 1H), 3.74, (s, 1H), 3.17 (br s, 1H), 2.46 (m, 1H), 2.32 (m, 1H), 1.95 (s, 3H), 1.89 (s, 3H), 1.82 (s, 6H), 1.05 (t, 3H), −0.22 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266910B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-91de6a9887ef43a081261629981047b1 |
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| Source note | uspto-grants-2016_02 |
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