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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044620Generated: 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/1044620

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Iodo-2-methoxyethaneHCID 79136—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(1R,4S)-methyl 4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylateHCID 10610130—
SolventTetrahydrofuranHCID 8028—
ProductMethyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylateHCID 5983358723%

Reaction Conditions

Temperature-78 °C

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 (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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563582B2
Source datasetuspto-grants-2013_10
ORD IDord-8cabd21508a74df0a61e286dd16ac49a
Source noteuspto-grants-2013_10