HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21503923, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Ethyl-9H-fluorene | HCID 274939 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 21503899 | HCID 21503899 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 21503923 | HCID 21503923 | — |
Reaction Steps
2-Butylfluorene (6.1 g.) was acetylated exactly as described for 2-ethylfluorene in the preceding Example 21, using acetic anhydride (3.08 g.) and aluminium chloride (8.66 g.) in dichloroethane. The product was recrystallised from light petroleum to give 2-acetyl-7-butylfluorene, m.p. 102°-104.5°. This product (1.98 g.) was oxidised with sodium hypobromite (from 7.23 g. of bromine and 4.52 g. sodium hydroxide in 160 ml. water) exactly as described for 2-acetyl-7-ethylfluorene in the preceding Example. The 7-butylfluorenone-2-carboxylic acid thus isolated had m.p. > 300° and was homogeneous by thin layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959482 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-6b102e6e31f6401fbd8b3e0a86ff4063 |
| Source note | uspto-grants-1976_05 |