HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983767Generated: October 30, 2026
Hydrochloric Acid → HCID 10729320, compound
https://huagongshe.com/reaction/983767
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | HCID 22556471 | HCID 22556471 | — |
| Reactant | HCID 178418365 | HCID 178418365 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10729320 | HCID 10729320 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06867161B1 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-dafd19e58cb84c2b972020dc288ff3cc |
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| Source note | uspto-grants-2005_03 |
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