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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097475Generated: October 31, 2026

Iodine → HCID 57571706, compound

https://huagongshe.com/reaction/2097475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 57571708HCID 57571708—
ReactantHCID 178418244HCID 178418244—
SolventDiethyl EtherHCID 3283—
ProductHCID 57571706HCID 57571706106.2%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To 76 ml of diethyl ether solution containing 24.1 g (84 mmol) of 1-bromo-2-cyclopropylmethoxy-3-methoxymethoxybenzene obtained in Reference example 12-(a) was added dropwise 53.4 ml (84 mmol) of 1.58M n-butyl lithium hexane solution at −60° C. or lower under argon atmosphere. The mixture was stirred at the same temperature for further 30 minutes, raised to −30° C., and then, 50 ml of diethyl ether solution containing 21.3 g (84 mmol) of iodine was added dropwise to the mixture. After completion of the dropwise addition, the mixture was stirred at the same temperature for 30 minutes, and then, gradually raised to room temperature. After completion of the reaction, to the reaction mixture was added 95 ml of 2% aqueous sodium thiosulfate solution, and the mixture was stirred for 1 hour. The organic layer after separation was washed with a saturated aqueous solution of sodium chloride, dried over dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 29.8 g of the title compound as a reddish oil substantially quantitatively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-d066b67e4fb841d783ff7518dd688aa5
Source noteuspto-grants-2013_05