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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225501Generated: October 25, 2026

Sodium Iodide → Allyl 4-iodomethyl-methyl-1-cyclohexanecarboxylate

https://huagongshe.com/reaction/2225501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium ThiosulfateHCID 24477—
ReactantAllyl 4-mesyloxymethyl-1-methyl-1-cyclohexanecarboxylateHCID 19004719—
SolventAcetoneHCID 180—
ProductAllyl 4-iodomethyl-methyl-1-cyclohexanecarboxylateHCID 1900469349.6%

Reaction Steps

5 g of sodium iodide was added to a solution of 2 g of allyl 4-mesyloxymethyl-1-methyl-1-cyclohexanecarboxylate (Example 45) in 50 ml of acetone. The solution was reacted for 4 hours, while it was refluxed. After reaction, 100 ml of an aqueous sodium thiosulfate solution was added to the reaction solution. The solution was extracted three times with 30 ml of ethyl acetate. The organic layer obtained was washed twice with an aqueous sodium thiosulfate solution and twice with an aqueous sodium chloride solution, and was dried over magnesium sulfate. Thereafter, the solvent was removed in vacuo. The oily substance obtained was subjected to column chromatography using 10 g of silica gel. From the fraction eluted with hexane and ethyl acetate=2:1, the solvent was removed in vacuo, yielding 1.1 g of allyl 4-iodomethyl-1-methyl-1-cyclohexanecarboxylate as a pale yellow oil, which had the following physiochemical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344845
Source datasetuspto-grants-1994_09
ORD IDord-f37a82d7fe964bbfa9bde494268ab89c
Source noteuspto-grants-1994_09