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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929454Generated: October 30, 2026

Diiodomethane → HCID 66849204, compound

https://huagongshe.com/reaction/929454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86667885HCID 86667885—
ReactantHCID 178418750HCID 178418750—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 66849204HCID 6684920477%

Reaction Steps

Trifluoroacetic acid (TFA; 281 mg, 2.47 mmol) was added to a solution of diethyl zinc (ZnEt2, 2.5 mL, 2.5M in hexane) in DCE (1 mL) at 0° C. and stirred for 35 mins. Diiodomethane (CH2I2, 66 mg, 2.5 mmol) was then added at 0° C., and the mixture stirred for an additional 20 min. A solution of (R)-5-(2-iodoallyl)-2,2,3,3,8,8,9,9-octamethyl-4,7-dioxa-3,8-disiladecane (step D; 188 mg, 0.41 mmol) in DCE (2 ml) was added and the reaction stirred at room temperature overnight. The reaction was then quenched by addition of a mixture of methanol (5 mL) and brine (0.5 mL). After stirring for an additional hour, the mixture was concentrated under reduced pressure. The crude material was extracted with aq.NH4Cl/CHCl3 and the organic layer washed with brine, dried (MgSO4) and concentrated under reduced pressure. The crude material was triturated in hexane and the solution filtered and evaporated to afford (R)-5-((1-iodocyclopropyl)methyl)-2,2,3,3,8,8,9,9-octamethyl-4,7-dioxa-3,8-disiladecane (148 mg, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296686B2
Source datasetuspto-grants-2016_03
ORD IDord-6b8f5e9b279b4827a5a6b330300fc4a3
Source noteuspto-grants-2016_03