HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052912Generated: October 30, 2026
Sodium hydride → Hept-5-ynoic acid methyl ester
https://huagongshe.com/reaction/2052912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 7-iodohept-5-ynoate | HCID 10901527 | — |
| Reactant | (R)-6-(tert-butyldimethylsilanyloxymethyl)-piperidin-2-one | HCID 58635302 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Hept-5-ynoic acid methyl ester | HCID 12079881 | — |
Reaction Steps
Sodium hydride (60% dispersion in oil, 195 mg, 4.87 mmol) was added to a solution of (R)-6-(tert-butyldimethylsilanyloxymethyl)-piperidin-2-one (1.13 g, 4.64 mmol) in DMF (8 mL) at rt. After 1 h, methyl 7-iodohept-5-ynoate (1.35 g, 5.07 mmol) in DMF (2 mL) was added via cannula. After 18 h at rt, the reaction was quenched by the addition of aqueous HCl (0.5 M, 25 mL) and the mixture was extracted with EtOAc (3×50 mL). The combined organic phase was washed with saturated aqueous NaHCO3 (50 mL) and brine (3×50 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→50% EtOAc/CH2Cl2, gradient) afforded 713 mg (40%) of 7-[(R)-2-tert-butyldimethylsilanyloxymethyl)-6-oxo-piperidin-1-yl]-hept-5-ynoic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07326716B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-7a39aed66fa240b595788cd3e596a335 |
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| Source note | uspto-grants-2008_02 |
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