HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261691Generated: October 25, 2026
1-Iodo-2-methoxyethane → Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylate
https://huagongshe.com/reaction/1261691
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Iodo-2-methoxyethane | HCID 79136 | — |
| 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-(2-methoxyethyl)cyclopent-2-ene-1-carboxylate | HCID 59833587 | 23% |
Reaction Steps
To a 1.00 M solution of lithium hexamethyldisilazide in tetrahydrofuran (9.1 mL, 9.1 mmol) under N2 at −78° C. was added a solution of methyl (1R,4S)-4-[(tert-butoxycarbonyl)amino]cyclopent-2-ene-1-carboxylate (1.0 g, 4.1 mmol) in tetrahydrofuran (2.0 mL). The resulted light brown solution was stirred at −78° C. for 30 min before adding a solution of 1-iodo-2-methoxyethane (0.93 g, 5.0 mmol) in tetrahydrofuran (2.0 mL). The mixture was stirred for an hour at −78° C. then kept in a freezer reading at −20° C. overnight. The reaction was quenched with saturated ammonium chloride. The layers were separated and the aqueous extracted with ether three times. The combined organics were then washed with brine, dried (magnesium sulfate), filtered and purified by flash chromatography (EtOAc/Hexane) to provide the desired product (0.28 g, 23%). LCMS calculated for C15H26NO5: (M+H) 300.2; found 300.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470827B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-b28bf8574a494abc991b652dee8c9fdd |
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| Source note | uspto-grants-2013_06 |
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