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HRID 1044620Erstellt: 26. Oktober 2026

1-Iodo-2-methoxyethane → Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylate

https://huagongshe.com/reaction/1044620

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Iodo-2-methoxyethaneHCID 79136—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt(1R,4S)-methyl 4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylateHCID 10610130—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylateHCID 5983358723%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

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 (MgSO4), filtered and purified by flash chromatography (EtOAc/Hexane) to provide the desired product (0.28 g, 23%). LCMS calculated for C5H26NO5: (M+H) 300.2; found 300.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08563582B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-8cabd21508a74df0a61e286dd16ac49a
Quellennotizuspto-grants-2013_10