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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65615Generated: October 28, 2026

Diethyl Ether → 2-Allyl-6-[(butylthio)methylene]-2-ethylcyclohexanone

https://huagongshe.com/reaction/65615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAllyl bromideHCID 7841—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-[(Butylthio)methylene]-6-ethylcyclohexanoneHCID 53766308—
SolventHexaneHCID 8058—
Product2-Allyl-6-[(butylthio)methylene]-2-ethylcyclohexanoneHCID 54503362—

Reaction Steps

To a well stirred solution of potassium tert-butoxide (17.95 g, 0.16 mole) in dry redistilled tert-butanol (160 ml) under nitrogen, 2-[(butylthio)methylene]6-ethylcylcohexanone (9.05 g, 0.04 mole), described in Example 3, is added slowly. The mixture is stirred at room temperature for 5 minutes and then chilled in an ice bath. Allyl bromide (21.8 g, 0.18 mole) is added rapidly to the chilled mixture. The mixture is then stirred at room temperature for 48 hr. Most of the solvent is then removed under reduced pressure and water (about 150 ml) is added. The aqueous solution is extracted with ether (3 ×). The combined ether extracts are washed with brine, dried (MgSO4) and concentrated to yield an oil. The oil is subjected to chromotography on silica gel (320 g) using 4% ether in hexane as eluant. Concentration of the eluate gives 2-allyl-6-[(butylthio)methylene]-2-ethylcyclohexanone, nmr(CDCl3) δ 0.85 (t, J=7, 3H), 2.85 (t, J=7, 2H), 4.80 - 6.0 (m, 3H), 7.5 (t, J=2, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04128560
Source datasetuspto-grants-1978_12
ORD IDord-cc9b0ea6a2494f1084cf3ac49292cdbb
Source noteuspto-grants-1978_12