HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fluorene → 2-(9H-fluoren-9-yl)ethane-1-thiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fluorene | HCID 6853 | — |
| Reactant | Thiirane | HCID 9865 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(9H-fluoren-9-yl)ethane-1-thiol | HCID 22407029 | 68.1% |
Reaction Steps
A solution of fluorene (20.0 g; 120 mmol) in THF (200 mL) was cooled to -40° C. and treated with 48 mL of a 2.5M solution of n-butyllithium in hexanes (120 mmol). After stirring for 15 minutes, a solution of ethylene sulfide (6.5 mL; 109 mmol) in 30 mL of THF was added, and the resulting mixture was stirred at -40° C. for 30 minutes and room temperature for 2 hours. The reaction was quenched by the addition of saturated ammonium chloride, the layers were separated, and the organic phase was washed with 10% HCl, dried and concentrated. The crude product was purified on a flash column, eluting with hexane, to provide 16.8 g (62%) of the product as an oil that recrystallized from hexane as a white solid, mp 38°-40° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05519043 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-d7ae73318a8c4e7c8630bf168d4ff67b |
| Source note | uspto-grants-1996_05 |