HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270538Generated: October 26, 2026
Isopropyl iodide → Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-isopropylcyclopent-2-ene-1-carboxylate
https://huagongshe.com/reaction/270538
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (1R,4S)-methyl 4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylate | HCID 10610130 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-isopropylcyclopent-2-ene-1-carboxylate | HCID 60122269 | 77.8% |
Reaction Steps
To a 1.00 M solution of lithium hexamethyldisilazide in THF (202 mL) at −78° C. was added a solution of methyl (1R,4S)4-[(tert-butoxycarbonyl)amino]cyclopent-2-ene-1-carboxylate (22.10 g, 91.59 mmol) in THF (36.2 mL) over 10 min. The solution was stirred at −78° C. for 30 min before isopropyl iodide (10.0 mL, 100 mmol) was added in one portion. The mixture was then moved to a freezer reading at −24° C. and kept overnight. The reaction was quenched with aqueous ammonium chloride and the resulting solution was extracted with ether three times. The ether layers were dried over sodium sulfate and evaporated in vacuo. The residue was purified by flash chromatography on silica eluting with 10% ethyl acetate/hexane to give the title compound (20.2 g). MS calculated for C15H25NO4: (M+H)+ 284; found 184.2 (M-Boc+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449467B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-18b0ba10ff6843cbaeca63fd60c915d1 |
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| Source note | uspto-grants-2008_11 |
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