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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637375Generated: October 25, 2026

Iodoethane → alpha-Cyclopentyl-p-methoxybutyrophenone

https://huagongshe.com/reaction/637375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantHCID 13175263HCID 13175263—
Solvent1,2-DimethoxyethaneHCID 8071—
Productalpha-Cyclopentyl-p-methoxybutyrophenoneHCID 131752642,888.9%

Reaction Steps

α-Cyclopentyl-p-methoxyacetophenone (13.0 g, 0.06 mol) was added slowly in dry DME (DME=Dimethoxyethane) to the suspension of NaH (8 g, 55-60% dispersion, 0.018 mmol) in dry DME under N2 atmosphere at room temperature. The suspension was stirred over night. Ethyl iodide (27.7 g, 0.18 mmol) was added and stirring continued for another two hours. Ice water was added cautiously and the water layer extracted with toluene. The organic layer was washed with water, dried and evaporated to give 12.7 g (0.0052 mol, 86%) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556677
Source datasetuspto-grants-1985_12
ORD IDord-2dd6c55b99864fc88ccca63a8507f669
Source noteuspto-grants-1985_12