HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoclidine → HCID 131727932, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoclidine | HCID 65630 | — |
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131727932 | HCID 131727932 | 22.1% |
Reaction Steps
(+/−)-3-Quinuclidinol benzoate (Sigma, 17.9 g, 77.5 mmol) was treated with L-tartaric acid (Aldrich, 99% ee, 11.63 g, 77.5 mmol) in EtOH (80%, 222 mL) at ambient temperature for 1 week. The white solid was filtered off and dried under reduced pressure. 6.5 g of 3-(R)-quinuclidinol benzoate·(L)-tartrate was obtained with ˜80% ee (assayed by HPLC. HPLC conditions: chiralpak AD column 25 cm×4 mm ID. solvent, EtOH:hexanes=15:85. flow rate, 1 mL/min. uv, 220 nm. Retention time: (S)-3-quinuclidinol benzoate, 7.87 min; (R)-3-quinuclidinol benzoate 13.3 min.) Recrystallization of the above solid in EtOH (80%, 35 mL) gave the title product (4.5 g, yield, 15%, >98% ee). MS (DCI/NH3) m/z 232 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674794B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-dce457631d4f486c9b37e93101bb4017 |
| Source note | uspto-grants-2010_03 |