Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | (+-)-Norketamine | HCID 123767 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (+-)-Norketamine | HCID 123767 | — |
| Product | HCID 86653325 | HCID 86653325 | — |
Reaction Steps
To a mixture of norketamine (0.05 g, 0.22 mmol) in anhydrous toluene (2 mL) and Na2CO3 (0.082 g) was added a solution of para-nitrophenyl chloroformate (0.129 g, 0.64 mmol) in anhydrous toluene (2 mL). After heating for 8 hours at 85° C., the reaction mixture was cooled to room temperature and filtered. Toluene was evaporated under vacuum and the reaction mixture was diluted with dichloromethane (DCM). The DCM layer was washed 6 times with 50% aqueous NaHCO3 solution to remove the para-nitrophenol side-product and then with brine. The DCM layer was then dried over anhydrous sodium sulfate, filtered, concentrated under vacuum to afford the para-nitrophenoxycarbamate of norketamine as a pale solid. 1H-NMR (CDCl3): δ 8.17 (2H, dd), 7.87 (1H, d), 7.37 (3H, m) 7.23 (2H, dd), 3.84 (1H, d), 2.55-1.71 (8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710070B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-fe8aac4101a64b3e9a260dfb6b254069 |
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| Source note | uspto-grants-2014_04 |
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