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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459063Generated: November 1, 2026

Iodine → (3r,5r)-3-Heptyl-5-iodomethyl-dihydrofuran-2-one

https://huagongshe.com/reaction/1459063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant(2R)-2-Heptyl-pent-4-enoic acidHCID 11041739—
SolventDiethyl EtherHCID 3283—
SolventOxolane--water (1/1)HCID 21881883—
Product(3r,5r)-3-Heptyl-5-iodomethyl-dihydrofuran-2-oneHCID 1090341871.1%

Reaction Steps

To a solution of 7.14 g (0.036 mol) of the product of Example 5 in 750 mL of THF/H2O (2:1), cooled to 0 degrees, was added 7.22 g (0.072 mol) of KHCO3 followed by 11.97 g (0.072 mol) of KI and then 18.30 g (0.072 mol) of iodine. The reaction was allowed to warm to room temperature and stirred for 18 h. The resulting mixture was diluted with ether and the organic layer was washed with aqueous sodium bisulfite solution, H2O and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with ethyl acetate/hexanes (1:10) to provide 8.30 g (71%) of the title compound and 3.36 g (29%) of the corresponding iodo-trans lactone as white solids. CI Mass Spec: 325.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852213
Source datasetuspto-grants-1998_12
ORD IDord-b4d2cb0fd3a04b658a6365e15cc4aad1
Source noteuspto-grants-1998_12