HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724497Generated: October 25, 2026
HCID 21880924, compound → HCID 21880978, compound
https://huagongshe.com/reaction/724497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21880924 | HCID 21880924 | — |
| Reactant | (2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodiethylsilane | HCID 67206735 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21880978 | HCID 21880978 | — |
Reaction Steps
At −78° C., n-butyllithium (1.56 M, 1.69 mL, 2.64 mmol) was added dropwise to a solution of 2,5-dimethylcyclopenta[1,2-b:4,3-b′]dithiophen (0.50 g, 2.42 mmol) in tetrahydrofuran (10 mL) and the mixture was stirred at room temperature for 4 hours. After the reaction mixture was cooled to −78° C., a solution of (2-allyloxy-3-tert-buyl-5-methylphenyl)chlorodiethylsilane (0.72 g, 2.20 mmol) in toluene (3 mL) was added dropwise thereto. The resulting reaction mixture was warmed to room temperature and stirred for 2 hours. After the solvent was distilled off under reduced pressure, toluene was added and the mixture was filtered to remove insoluble substances. The filtrate was concentrated under reduced pressure to quantitatively obtain (2-allyloxy-3-tert-butyl-5-methylphenyl)(2,5-dimethylcyclopenta[1,2-b:4,3-b′]dithiophen-7-yl)diethylsilane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07141690B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-eb56857b284943b4b1889f27cb0c9984 |
|---|
| Source note | uspto-grants-2006_11 |
|---|