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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094825Generated: November 1, 2026

Diiodomethane → HCID 57582366, compound

https://huagongshe.com/reaction/1094825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantHCID 57582372HCID 57582372—
ReactantHCID 178418750HCID 178418750—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 57582366HCID 575823669%

Reaction Steps

Diethyl zinc (1M in toluene, 23 ml, 23 mmol) was added under nitrogen with stirring to a solution of 2-bromo-4-fluoro-1-vinyloxy-benzene (Preparation 88, 1.0 g, 4.61 mmol) in dichloroethane (45 ml) at −10° C. (ice-salt-MeOH), taking care to maintain the temperature below 0° C. Diiodomethane (6.17 g, 23 mmol) in dichloroethane (10 ml) was then added via a syringe to the reaction mixture over 5 minutes ensuring that the reaction mixture remained at a temperature below +5° C. (internal temp). The reaction mixture was stirred at this temperature for twenty minutes and then allowed to attain room temperature and stirring was continued for 72 hours. The reaction was quenched with cold saturated ammonium chloride (aqueous solution) (5 ml) then the lower organic phase was removed, whilst the aqueous was extracted with a further dichloromethane (20 ml). The combined organic layers were dried over anhydrous Na2SO4 (s), filtered and evaporated in vacuo. Purification by column chromatography on silica gel eluting with tert-butyldimethyl ether:heptane 1:99 to 1:19 afforded almost pure title compound (93 mg, 9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134007B2
Source datasetuspto-grants-2012_03
ORD IDord-8a1eb565cc0346f98cafc7d7ccc5b971
Source noteuspto-grants-2012_03