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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038775Generated: November 1, 2026

N-Iodosuccinimide → [1-(5-Iodo-furan-2-yl)-cyclopropyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2038775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactanttert-Butyl (1-(furan-2-yl)cyclopropyl)carbamateHCID 67117129—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventSodium ThiosulfateHCID 24477—
Product[1-(5-Iodo-furan-2-yl)-cyclopropyl]-carbamic acid tert-butyl esterHCID 6711573272.7%

Reaction Steps

To a solution of (1-furan-2-yl-cyclopropyl)-carbamic acid tert-butyl ester (4.30 g, 19.3 mmol) in anhydrous DMF (77 mL) at room temperature was added N-iodosuccinimide (4.77 g, 21.2 mmol) as a solid in one portion. The reaction was stirred for 2.5 h over which time a deep red color developed. The reaction was diluted with sat. aq. Na2S2O3 (75 mL), water (75 mL), and diethyl ether (100 mL). The layers were separated and the aqueous layer was extracted with diethyl ether (2×100 mL). The combined organic layers were dried over Na2SO4 and concentrated. The resultant solids were triturated with hexanes to give 4.9 g [1-(5-iodo-furan-2-yl)-cyclopropyl]-carbamic acid tert-butyl ester as a light yellow powder, m/z 350.5 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575360B2
Source datasetuspto-grants-2013_11
ORD IDord-55af917f52c4430ca644bccc249ddb0d
Source noteuspto-grants-2013_11