HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415842Generated: November 4, 2026
Water → 9-(4-bromobutyl)-9H-fluorene-9-carboxylic acid
https://huagongshe.com/reaction/2415842
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,3-Dibromobutane | HCID 21508 | — |
| Reactant | 9-Carboxyfluorene | HCID 74809 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 9-(4-bromobutyl)-9H-fluorene-9-carboxylic acid | HCID 10712518 | — |
Reaction Steps
89 ml (0.11 mol) of a 1.6-Molar n-butyl-lithium solution in hexane are added dropwise to a solution of 21 g (0.1 mol) of 9-fluorenecarboxylic acid in 700 ml of tetrahydrofuran at 0° C. under nitrogen and stirred for one hour. Then, again at 0° C., 13.13 ml (0.11 mol) of dibromobutane are added and the solution is stirred for 30 hours at ambient temperature. After this time 50 ml of water are added and the mixture is stirred for 30 minutes. The solution is concentrated by evaporation, mixed with water and extracted with 250 ml of diethylether. The aqueous phase is acidified with 150 ml of 1N hydrochloric acid and extracted three times with 250 ml of dichloromethane. The combined organic phases are dried over sodium sulphate and the solvent is eliminated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06821967B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-5ad7f00898934cb99cf26cf55d726437 |
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| Source note | uspto-grants-2004_11 |
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