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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183203Generated: November 1, 2026

N-Iodosuccinimide → HCID 69478504, compound

https://huagongshe.com/reaction/1183203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86664898HCID 86664898—
CatalystTrifluoroacetic acidHCID 6422—
SolventDichloromethaneHCID 6344—
ProductHCID 69478504HCID 6947850417.3%

Reaction Steps

To a solution of ethyl (1S,2S)-2-{4-[1-(2-fluoroethyl)-1H-imidazol-4-yl]phenyl}cyclopropanecarboxylate (450 mg, 1.488 mmol) in dichloromethane (5 mL) was added N-iodosuccinimide (352 mg, 1.563 mmol) and three drops trifluoroacetic acid. The reaction was stirred at rt for 3 h. The mixture was neutralized with aqueous sodium bicarbonate and the organics were extracted with dichloromethane. The organics were then washed with aqueous sodium thiosulfate, followed by three washes with water. The organics were dried (MgSO4), concentrated, and purified on 20 g of silica gel eluting a gradient of 35-100% ethyl acetate in hexanes to give rise to the title compound as a brown oil (110 mg, 0.257 mmol). LCMS: [M+1]+=429.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664253B2
Source datasetuspto-grants-2014_03
ORD IDord-d38cf30e76554b9f8ac7bce9d14cdf6d
Source noteuspto-grants-2014_03