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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
Reactant1-tert-Butyl 2-methyl (2S)-piperidine-1,2-dicarboxylateHCID 10824139—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDichloromethaneHCID 6344—
ProductHCID 53718989HCID 5371898965%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06228872B1
Source datasetuspto-grants-2001_05
ORD IDord-438f68bbb1c847b1964fca31bd2085f9
Source noteuspto-grants-2001_05