Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 68442560 | HCID 68442560 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Solvent | Benzyl chloroformate | HCID 10387 | — |
| Product | HCID 68442773 | HCID 68442773 | — |
Reaction Steps
A mixture of 1.2 g (2S,4R,5R)-5-hydroxy-4-(4-methoxy-phenyl)-piperidine-2-carboxylic acid ethyl ester in 40 ml of ethyl acetate, 20 ml of saturated aqueous sodium carbonate solution and 0.42 ml of benzyl chlorformate is stirred for 1 hour at 0° C., diluted with ethyl acetate and the organic phase is dried over sodium sulfate. The organic phase is concentrated under reduced pressure and the residue is purified by flash chromatography (SiO2 60 F) to afford the title compound as a yellow oil. Rf=0.3 (EtOAc-heptane 1:1); Rt=4.34.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687495B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-d41e86abfeeb476d8d62520af53c1d80 |
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| Source note | uspto-grants-2010_03 |
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