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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662042Generated: October 30, 2026

Dimethylformamide → methyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate

https://huagongshe.com/reaction/1662042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant(1S,2R)-2-(tert-Butoxycarbonylamino)cyclopentanecarboxylic acidHCID 1268163—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productmethyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylateHCID 11322482—

Reaction Steps

To a mixture of (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylic acid (0.88 g) and DMF (8.0 ml) were added cesium carbonate (2.5 g) and methyl iodide (0.82 g) under ice-cooling, followed by stirring at room temperature for 1.5 hours. To the reaction mixture ethyl acetate and water under ice-cooling were added. The organic layer was separated, the aqueous layer was extracted with ethyl acetate (15 ml), and the organic layer was combined and washed with a 10% aqueous citric acid solution, a saturated sodium bicarbonate solution, water, and saturated brine in this order. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain methyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate (0.85 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030489B2
Source datasetuspto-grants-2011_10
ORD IDord-82c1eec8dd9d4bc5989d5ae1abf11802
Source noteuspto-grants-2011_10