HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrophosphoric acid → HCID 178520530, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrophosphoric acid | HCID 1023 | — |
| Reactant | Bis(eta-cyclopentadienyl) iron | HCID 7611 | — |
| Reactant | Butyl ether | HCID 8909 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromobutyric acid | HCID 75809 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178520530 | HCID 178520530 | 82.1% |
Reaction Steps
6.68 g of 4-bromobutyric acid, 1.86 g of ferrocene, 20 g of pyrophosphoric acid, 20 g of polyphosphoric acid, and 20 ml of di n-butylether were added and stirred while heating at 50° to 60° C. for 3 hours, then poured into water, made to be basic with sodium hydroxide, extracted with methylene chloride, and dried. The unreacted-ferrocene was removed with column chromatography, to obtain 2.75 g of 3-bromopropylferrocenyl ketone presented by the formula (D), in a yield of 82.0%. The proton nuclear magnetic resonance (1H--NMR) spectrum of the product is shown in FIG. 4. The result showed that the resulting product was the desired product (3-bromopropylferrocenyl ketone). ##STR11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05110964 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-8c690e8881d14c39aeb12f0f8e770b4a |
| Source note | uspto-grants-1992_05 |