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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83517Generated: October 30, 2026

Pyridine → (R)-2-Oxoimidazolidine-1,5-dicarboxylic Acid 1-benzyl ester 5-tert-butyl Ester

https://huagongshe.com/reaction/83517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium AcetateHCID 517045—
Reactant(4R)-3-[(Benzyloxy)carbonyl]-2-oxoimidazolidine-4-carboxylic acidHCID 688195—
SolventChloroformHCID 6212—
Solventtert-ButanolHCID 6386—
Product(R)-2-Oxoimidazolidine-1,5-dicarboxylic Acid 1-benzyl ester 5-tert-butyl EsterHCID 51425954—

Reaction Steps

To a solution of (R)-2-oxoimidazolidine-1,5-dicarboxylic acid 1-benzyl ester (534 mg) in chloroform (2.6 ml) were sequentially added pyridine (1.0 ml) and tert-butylalcohol (1.5 ml) at room temperature, and the mixture was stirred. This reaction solution was iced, and phosphorous oxychloride (0.23 ml) was added thereto, and then the mixture was stirred at room temperature for 5 hours. This reaction solution was iced, and a 20 wt % aqueous solution of sodium acetate (20 ml) was added thereto, and then chloroform (5 ml) was further added at room temperature, and the mixture was stirred for 30 minutes. This mixed solution was extracted with chloroform, and the resulting organic layer was washed with a 0.1M aqueous solution of hydrochloric acid, water, a saturated aqueous solution of sodium hydrogen carbonate and a saturated aqueous solution of sodium chloride, and then dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give a crude product of the titled compound (467 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846746B2
Source datasetuspto-grants-2014_09
ORD IDord-050e667941c042f1a9a63cc20ed78f75
Source noteuspto-grants-2014_09