HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Carboxybutyl)triphenylphosphonium bromide → HCID 86747752, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Carboxybutyl)triphenylphosphonium bromide | HCID 161236 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86747751 | HCID 86747751 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86747752 | HCID 86747752 | — |
Reaction Steps
(4-Carboxybutyl)triphenylphosphonium bromide (22.03 g) and potassium t-butoxide (1-M, 99.4 ml) were treated in THF (100 ml) to give a ylide, to which was added the previously obtained lactol (58) at 0° C., and the mixture was kept at room temperature overnight. The reaction was worked up in the usual manner to give the carboxylic acid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05302617 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-ba122d84737e46a88fa9828a039173e5 |
| Source note | uspto-grants-1994_04 |