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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975017Generated: October 29, 2026

Sodium Bicarbonate → Benzyl 2-(3-hydroxyprop-1-en-1-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/975017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 53843982HCID 53843982—
ReactantPhenylmethyl 2-(3-ethoxy-3-oxo-1-propen-1-yl)-1-piperidinecarboxylateHCID 54132542—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 2-(3-hydroxyprop-1-en-1-yl)pyrrolidine-1-carboxylateHCID 4266884—
Product1-(N-benzyloxycarbonyl-piperid-2-yl)-3-hydroxypropeneHCID 54420541—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of either ethyl 3-(N-benzyloxycarbonylpyrrolidin-2-yl)-2-propenoate or ethyl-3-(N-benzyloxycarbonylpiperid-2-yl)-2-propenoate (R, or S, or racemate, 10.00 mmol) in anhydrous tetrahydrofuran (75 mL) at -78° C. under nitrogen was added dropwise a solution of diisobutylaluminium hydride (1.0M in hexanes, 12.0 mL, 22.0 mmol, 2.2 eq). The resulting solution was stirred at -78° C. under nitrogen for 30 minutes. The reaction solution was then allowed to warmed to room temperature over the course of 2 hours. A saturated solution of sodium hydrogen carbonate (50 mL) was added, and the aqueous mixture was extracted with ethyl acetate (3×50 mL). The extracts were combined, dried (MgSO4), and evaporated under reduced pressure. Column chromatography of the residue with diethyl ether/hexanes [1:1] afforded either 1-(N-benzyloxycarbonylpyrrolidin-2-yl)-3-hydroxypropene or 1-(N-benzyloxycarbonyl-piperid-2-yl)-3-hydroxypropene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607951
Source datasetuspto-grants-1997_03
ORD IDord-cc67781cb23345f69fa801283cf75952
Source noteuspto-grants-1997_03