Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethyl [3-(3-chlorophenyl)-2-oxopropyl]phosphonate | HCID 12989750 | — |
| Reactant | HCID 86595300 | HCID 86595300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11212242 | HCID 11212242 | 68.4% |
Reaction Steps
Sodium hydride (60% dispersion in oil, 15 mg, 0.39 mmol) was added to a solution of [3-(3-chlorophenyl)-2-oxopropyl]-phosphonic acid dimethyl ester (97 mg, 0.35 mmol) in THF (1.5 mL) at 0° C. After 1 h at 0° C., a solution of [4-((R)-2-formyl-6-oxo-piperidin-1-yl)-but-2-ynyloxy]-acetic acid methyl ester (0.37 mmol, crude) in THF (1.5 mL) was added via cannula. The reaction was allowed to warm to rt. After 18 h at rt, the reaction was quenched with aqueous acetic acid (50%, 15 mL) and extracted with EtOAc (3×15 mL). The combined organic phase was washed with brine (20 mL), dried (MgSO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (20% →30% EtOAc/CH2Cl2, gradient) afforded 100 mg (68%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179820B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-5ae0d8fd4f2d47989293239b2f7200e8 |
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| Source note | uspto-grants-2007_02 |
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