HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266831Generated: October 26, 2026
Hydrochloric Acid → HCID 70048066, compound
https://huagongshe.com/reaction/266831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-[1-(4-Formylbenzoyl)-4-piperidinyl]-3,4-dihydrocarbostyril | HCID 19030828 | — |
| Product | HCID 70048066 | HCID 70048066 | — |
Reaction Steps
4-Hydroxypropyltriphenylphosphonium bromide (2.4 g) is dispersed into tetrahydrofuran (50 ml) and thereto is added dropwise lithium diisopropylamide (a solution in 1.99N tetrahydrofuran) (6.1 ml) at 0°-5° C. After adding, the mixture is stirred at 0°-5° C. for 1 hour and thereto is added 1-[1-(4-formylbenzoyl)-4-piperidinyl]-3,4-dihydrocarbostyril (2 g). The mixture is stirred at room temperature overnight. The reaction mixture is poured into ice-water and adjusted to pH 4-5 by adding conc. hydrochloric acid. The mixture is extracted with ethyl acetate and dried with magnesium sulfate. The solvent is distilled off and the resulting residue is purified by silica gel column chromatography (solvent: n-hexane:ethyl acetate=1:1→ethyl acetate:methanol=20:1) to give 1-{1-[4-(4-hydroxy-1-butenyl)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05652247 |
|---|
| Source dataset | uspto-grants-1997_07 |
|---|
| ORD ID | ord-d3816f7a1790441691806e24bce93e86 |
|---|
| Source note | uspto-grants-1997_07 |
|---|