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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374295Generated: October 31, 2026

Diethyl Ether → benzyl (S)-2-oxo-1-((1S,2R)-4-oxo-2-propylcyclohexyl)pyrrolidin-3-ylcarbamate

https://huagongshe.com/reaction/1374295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 86596863HCID 86596863—
SolventAcOH THF waterHCID 21877175—
Productbenzyl (S)-2-oxo-1-((1S,2R)-4-oxo-2-propylcyclohexyl)pyrrolidin-3-ylcarbamateHCID 8659686437.3%

Reaction Steps

Examples 2t and 2u, Step 5: A sample of benzyl (S)-1-((1S,2R,4R)-4-(tert-butyldimethylsilyloxy)-2-propylcyclohexyl)-2-oxopyrrolidin-3-ylcarbamate (0.4 g, 0.82 mmol) was dissolved in 36 mL of 4:1:1 HOAc/THF/water and stirred at RT for 5 days. The volatiles were removed in vacuo and the residue was dissolved in EtOAc. The organic phase was washed with sat. NaHCO3, dried (MgSO4), filtered, and concentrated in vacuo. The residue was dissolved in methylene chloride (4 mL) and the resultant solution was cooled to 0° C. and charged with Dess-Martin periodinane (0.54 g, 1.27 mmol). After stirring for 2 h at RT, the solution was again cooled to 0° C. and charged with Dess-Martin periodinane (0.27 g). The reaction was stirred at RT for 14 h and treated with Et2O. The resultant suspension was washed with 1 N NaOH, sat. Na2S2O3, and sat. NaHCO3. The organic phase was dried (MgSO4), filtered, and concentrated in vacuo to afford benzyl (S)-2-oxo-1-((1S,2R)-4-oxo-2-propylcyclohexyl)pyrrolidin-3-ylcarbamate (114 mg). MS found: (M+Na)+=395.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163937B2
Source datasetuspto-grants-2007_01
ORD IDord-cab4e875be7a417c81fc802de4ea2654
Source noteuspto-grants-2007_01