HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 53888575, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 53785538 | HCID 53785538 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 53888575 | HCID 53888575 | — |
Reaction Steps
Under a nitrogen blanket and at 90° C., 2 g (9.2 mmol) of the acetylene derivative from Example 1 is added to a mixture of 50 mg of copper(II) chloride, 110 mg of palladium(II) acetate, 380 mg of triphenylphosphine and 2.6 g (18.4 mmol) of benzoyl chloride in 100 ml of triethylamine. After 30 minutes, the mixture is allowed to cool and the solid is filtered off. The filtrate is evaporaed down, and the residue is taken up in methyl tert-butyl ether, washed with water, dried and evaporated down. The residue is stirred with diethyl ether and the precipitated pale brown solid is filtered off. 2.0 g (68%) of compound 26, Table 6, remain. Mp. 89°-94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05449809 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-80039718d68840cc9de077346c36ae5f |
| Source note | uspto-grants-1995_09 |