HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358057Generated: November 1, 2026
Phosphorus oxychloride → HCID 178424888, compound
https://huagongshe.com/reaction/1358057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 178424889 | HCID 178424889 | — |
| Catalyst | Benzyltriethylammonium bromide | HCID 165294 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178424888 | HCID 178424888 | 15.6% |
Reaction Steps
0.97 g (3.24 mmol) of 1′,2′,3′,4′,5′-pentamethylferrocene-1-carboxylic acid is converted into the acid chloride by reaction with 0.683 g (3.28 mmol) of phosphorus pentachloride in 30 ml of toluene, as described by B. Bildstein, A. Hradsky, H. Kopacka, R. Malleier, K. H. Ongania, J. of Organomet. Chem. 540 (1997) 127. After stirring for six hours, toluene, phosphorus oxytrichloride and the other volatile constituents are taken off in a high vacuum. The resulting residue is dissolved in 30 ml of absolute toluene and reacted with 0.21 g (3.24 mmol) of sodium azide in the presence of 0.737 g (3.24 mmol) of benzyltriethylammonium bromide as phase transfer catalyst to form 1′,2′,3′,4′,5′-pentamethylferrocene-1-carboxylic acid azide. After stirring overnight, an aqueous work-up is carried out and the product is chromatographed (Al2O3, eluant: petroleum ether/ether 1:1). In addition to 0.13 g of 1′,2′,3′,4′,5′-pentamethylferrocene-1-carboxylic acid azide, 0,2 g of 1′,2′,3′,4′,5′-pentamethylferrocene-1-carboxylic acid is recovered, corresponding to a conversion of 0.77 g (2.56 mmol) of carboxylic acid into 0.13 g of acid azide in a yield of 15.6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06593437B1 |
|---|
| Source dataset | uspto-grants-2003_07 |
|---|
| ORD ID | ord-1a0313e8e737414f9b31c8e148902e5b |
|---|
| Source note | uspto-grants-2003_07 |
|---|