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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (1S,2R)-2-(tert-Butoxycarbonylamino)cyclopentanecarboxylic acid | HCID 1268163 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030489B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-82c1eec8dd9d4bc5989d5ae1abf11802 |
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| Source note | uspto-grants-2011_10 |
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