Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Quinuclidinone | HCID 19507 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | tert-butyl (2S)-2-amino-3-phenylpropanoate | HCID 6931633 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Quinuclidinol hydrochloride | HCID 2723725 | 74% |
Reaction Steps
To a solution of 9.00 g (56.25 mmol) 3-quinuclidinone and 4.15 g (18.75 mmol) Phe-O-t-Bu in 50 ml methanol was added over a 12 hour period a solution of 2.95 g (46.9 mmol) sodium cyanoborohydride in 13 ml methanol. After stirring for an additional 8 hours, 5.78 g (50.0 mmol) pyridine hydrochloride was added and after 11/2 hours stirring, sodium chloride was removed by filtration. The filtrate was concentrated to a foam which was treated with 15 ml methanol and 50 ml ethyl acetate to give a slurry of the byproduct 3-hydroxy quinuclidine hydrochloride (74% of excess) which was removed by filtration. The filtrate was concentrate to an oil and charged with 10 ml methanol to a 5×200 cm column of LH-20 and eluted with methanol. The product fraction contained 6.54 g of a mixture of diastereomers in a 55:45 ratio as established by HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05194605 |
|---|
| Source dataset | uspto-grants-1993_03 |
|---|
| ORD ID | ord-bb5bf95155a544759cea26a6a40025e8 |
|---|
| Source note | uspto-grants-1993_03 |
|---|