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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983767Generated: October 30, 2026

Hydrochloric Acid → HCID 10729320, compound

https://huagongshe.com/reaction/983767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantHCID 22556471HCID 22556471—
ReactantHCID 178418365HCID 178418365—
CatalystHCID 178460666HCID 178460666—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10729320HCID 1072932077%

Reaction Conditions

Temperature-50 °C

Reaction Steps

To an ethyl ether solution (12 ml) containing 3-[(ethoxycarbonyl)oxy]-1,2-nonadiene (424 mg, 2.0 mmol) and tetraisopropoxytitanium (0.89 ml, 3.0 mmol) was added at −78° C. an ethyl ether solution containing isopropylmagnesium bromide (6.0 mmol). The reaction liquid was heated to −50° C. over 30 minutes and stirred for 1 hour. The reaction liquid was given dropwise a tetrahydrofuran solution (4 ml) containing iodine (761 mg, 3.0 mmol). After heating to 0° C. over 1.5 hours, the reaction liquid was given 3N hydrochloric acid (4 ml) and separated into layers. The organic layer was washed with a saturated aqueous solution of sodium thiosulfate and a saturated aqueous solution of sodium hydrogen carbonate, dried with anhydrous magnesium sulfate, and freed of solvent by vacuum distillation. The residues were purified by silica gel chromatography. There was obtained 385 mg of (E)-2-iodo-1,3-nonadiene as an iodinated compound (yield: 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867161B1
Source datasetuspto-grants-2005_03
ORD IDord-dafd19e58cb84c2b972020dc288ff3cc
Source noteuspto-grants-2005_03