HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Hydroxyphenylacetylene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ritodrine | HCID 33572 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Monosilylacetylene | HCID 136821 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Hydroxyphenylacetylene | HCID 10909551 | 60% |
Reaction Steps
In recent year, Polymer. Prepar. 1993, 34(1), 511-12. and Japanese Laid Open Patent HEI 8-217698 have described a process that 3- or 4-halophenol having a protected hydroxyl group, when necessary, is subjected to coupling with trimethylsilylacetylene or other monosilylacetylene in a triethylamine solvent in the presence of a palladium catalyst and thereafter subjected to removing of the silyl group and where necessary, deprotecting of the hydroxyl group to obtain desired hydroxyphenylacetylene in a considerably high yield of 60 to 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127583 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-62a95325c1e345c7bede9dc12f967120 |
| Source note | uspto-grants-2000_10 |