HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → rel-1-(1,1-Dimethylethyl) 3-methyl (3R,5S)-1,3,5-piperidinetricarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | (3S,5R)-1-(tert-butoxycarbonyl)-5-(methoxycarbonyl)piperidine-3-carboxylic acid (1R)-1-phenylethylamine salt | HCID 86680826 | — |
| Solvent | Water | HCID 962 | — |
| Product | rel-1-(1,1-Dimethylethyl) 3-methyl (3R,5S)-1,3,5-piperidinetricarboxylate | HCID 11358159 | 96.1% |
Reaction Steps
(3S,5R)-1-(tert-Butoxycarbonyl)-5-(methoxycarbonyl)piperidine-3-carboxylic acid (1R)-1-phenylethylamine salt (20.0 g, 49.0 mmol), methanol (20 mL) and water (80 mL) were charged. A solution of citric acid (11.3 g, 58.8 mmol) in water (20.0 mL) was added dropwise at 20-30° C., and the mixture was stirred at the same temperature for 1.5 hr. The precipitated crystals were collected by filtration, washed with water (60 mL), and dried under reduced pressure at 50° C. to give (3S,5R)-1-(tert-butoxycarbonyl)-5-(methoxycarbonyl)piperidine-3-carboxylic acid as a white crystalline powder (13.5 g, yield 96.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09018374B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-f52f1c3a6adf4c6bb12d934e2913e97c |
| Source note | uspto-grants-2015_04 |