HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599372Generated: November 1, 2026
Potassium Carbonate → HCID 131720616, compound
https://huagongshe.com/reaction/1599372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | O-Desmethylquinidine | HCID 51196 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131720616 | HCID 131720616 | 94.3% |
Reaction Steps
To a solution of 400 mg (1.2 mmol) of 6-hydroxycinchonane (1) in 25 ml of anhydrous acetone (dried and distilled over potassium carbonate) and 5 ml of anhydrous dimethylformamide was added 267 mg (1.93 mmol) of anhydrous potassium carbonate followed by 129 ml (0.87 mmol) of 4-bromobutyronitrile and a catalytic amount (3 mg) of 18-crown-6. The reaction mixture was heated to reflux for 18 h, cooled and filtered. The filtrate was concentrated under reduced pressure and redissolved in 200 ml of chloroform. The organic layer was washed with 2×50 ml of 5% aqueous sodium hydroxide, washed with brine, dried using anhydrous magnesium sulfate and yielded 310 mg (0.82 mmol, 66%) of (9S)-4-[(9-hydroxycinchonan-6'-yl)oxy]butanenitrile (2) as pale yellow solids. MS, IR and NMR data confirmed the identity of the compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05741715 |
|---|
| Source dataset | uspto-grants-1998_04 |
|---|
| ORD ID | ord-e8cce4fa393d4fd1a3c64059dad37b66 |
|---|
| Source note | uspto-grants-1998_04 |
|---|