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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393346Generated: October 29, 2026

tert-butyl(2S)-2-[4-(hydroxymethyl)-2-oxo-1-pyrrolidinyl]butanoate → 1-[(1S)-1-(tertbutoxycarbonyl)propyl]-5-oxo-3-pyrrolidinecaboxaldehyde

https://huagongshe.com/reaction/393346

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl(2S)-2-[4-(hydroxymethyl)-2-oxo-1-pyrrolidinyl]butanoateHCID 57478730—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product1-[(1S)-1-(tertbutoxycarbonyl)propyl]-5-oxo-3-pyrrolidinecaboxaldehydeHCID 1834611649.7%

Reaction Steps

In a three necked flask, under argon, a solution of tert-butyl (2S)-2-[4-(hydroxymethyl)-2-oxo-1-pyrrolidinyl]butanoate 398 (4.0 g, 0.016 mol.) in CH2Cl2 (8 ml) is added to a suspension of CrO3 (6.2 g, 0.062 mol.) in pyridine (11.3 ml)/CH2Cl2 (80 ml) stirred at room temperature. The temperature increases to 30° C. and the suspension is stirred for 0.2 h. The suspension is filtered through celite and the filtrate is washed successively with HCl 1N, brine, dried over magnesium sulfate and concentrated in vacuo to afford the crude aldehyde which is purified by column chromatography on silicagel (hexane/acetone 70/30 (v/v)) to afford 2.03 g of 1-[(1S)-1-(tertbutoxycarbonyl)propyl]-5-oxo-3-pyrrolidinecaboxaldehyde 396 (41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806287B2
Source datasetuspto-grants-2004_10
ORD IDord-1fd55854b1c345f2abff266f01b4cf6e
Source noteuspto-grants-2004_10