HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976613Generated: October 29, 2026
Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → HCID 53718989, compound
https://huagongshe.com/reaction/1976613
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| Reactant | 1-tert-Butyl 2-methyl (2S)-piperidine-1,2-dicarboxylate | HCID 10824139 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53718989 | HCID 53718989 | 65% |
Reaction Steps
A stirred solution of (S)-N-(t-butoxycarbonyl)-pipecolinic acid methyl ester (2.04 g, 8.39 mmol) in methylene chloride (75 mL) at −78° C. under nitrogen was treated with diisobutylaluminum hydride (1.0 M in toluene, 14.2mL, 14.2 mmol). After 1.25 h a second aliquot of diisobutylaluminum hydride (2.00 mL, 2.00 mmol) was added. The mixture was stirred for an additional 30 min. and then quenched by the addition of a 20% aqueous Rochelle's salt solution (100 mL) followed by vigorous stirring for 1 h. The aqueous layer was extracted with methylene chloride and the combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The crude aldehyde was dissolved in methylene chloride (100 mL) and treated with methyl (triphenylphosphoranylidene)acetate (4.00 g, 12.0 mmol). After 15 hours (h) the reaction mixture was concentrated and purified by flash chromatography to give the desired product (1.46 g, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06228872B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-438f68bbb1c847b1964fca31bd2085f9 |
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| Source note | uspto-grants-2001_05 |
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