Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73393Generated: October 26, 2026

Allyl iodide → Butyl 1-allylcyclopropane-1-sulfonate

https://huagongshe.com/reaction/73393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantButyl cyclopropanesulfonateHCID 10464888—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductButyl 1-allylcyclopropane-1-sulfonateHCID 5938637669%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-butyl cyclopropanesulfonate (4.8 g, 24.9 mmol) in THF at −78° C. was added simultaneously butyllithium solution (15.6 ml, 24.9 mmol, 1.6M, THF) and allyl iodide (24.9 mmol) under nitrogen atmosphere. The reaction mixture was stirred 2 hours at −78° C. and 3 hours at room temperature. The volatiles were evaporated under reduced pressure and the residue extracted with CH2Cl2 (100 ml). The extract was washed with water, dried (MgSO4) and evaporated. The residue was purified over silica gel chromatography (eluants: hexane/CH2Cl2) to obtain the titled product (3.75 g, 69.0%) as a colorless oil, 1H NMR (300 MHz, CDCl3): δ 5.6 (m, 1H), 5.13-5.08 (t, 2H), 4.21 (t, 2H), 2.65 (d, 2H), 1.7 (m, 2H), 1.4 (m, 4H), 0.93 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829052B2
Source datasetuspto-grants-2014_09
ORD IDord-d91d8ed404e84d39b56aac3d09d5d6d1
Source noteuspto-grants-2014_09