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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182836Generated: October 26, 2026

Diiodomethane → 1-Trimethylsiloxybicyclo[4.1.0]heptane

https://huagongshe.com/reaction/2182836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantAmmonium ChlorideHCID 25517—
ReactantCyclohexene, 1-((trimethylsilyl)oxy)-HCID 81161—
ReactantHCID 178418750HCID 178418750—
SolventHexaneHCID 8058—
Product1-Trimethylsiloxybicyclo[4.1.0]heptaneHCID 1106309463%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diiodomethane(120 μl, 1.5 mmol) was added slowly to perfluorohexanes (FC-72, 3 mL) in a test tube (14 mm×105 mm) and then trimethylsiloxycyclohexene (180 mg, 1.05 mmol) in hexane (3.5 mL) was slowly poured into the test tube. A hexane solution of diethylzinc (1.0 M, 1.5 mmol, 1.5 mmol) was added to the hexane layer, and the diiodomethane layer on the bottom was stirred gently so as not to mix the three phases. After 10 h at room temperature, additional diidomethane (40 μl, 0.5 mmol) was added to the bottom layer of the test tube by using a syringe. After 14 h, the reaction mixture was cooled to 0° C., and saturated NH4Cl (10 mL) was added. The hexane layer was decanted, washed with H2O, dried over MgSO4, and concentrated in vacuo. The residue was purified by short column chromatography (17 mm×20 mm of florisil layer over 50 mm of silica gel layer) with benzene/hexane: ¼ to give 1-trimethylsiloxybicyclo[4.1.0]heptane in 63% yield (123 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897331B2
Source datasetuspto-grants-2005_05
ORD IDord-92a0f2960a1748639a894db00f443c92
Source noteuspto-grants-2005_05