HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594887Generated: October 30, 2026
Tetrahydrofuran → HCID 86724288, compound
https://huagongshe.com/reaction/594887
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86724289 | HCID 86724289 | — |
| Catalyst | mu-Chlorobis(eta5-cyclopentadienyl)(dimethylaluminum)-mu-methylenetitanium | HCID 53384502 | — |
| Product | HCID 86724288 | HCID 86724288 | — |
Reaction Steps
To a solution of 6-bromo-4H-spiro[chromene-3,3′-oxetan]-4-one (143 mg, 0.531 mmol) in THF (2 mL) was added Tebbe reagent ((C5H5)2TiCH2ClAl(CH3)2, μ-Chloro[di(cyclopenta-2,4-dien-1-yl)]dimethyl(μ-methylene)titaniumaluminum, 0.5 M in toluene, 2 mL) under ice-water bath cooling. After the reaction mixture was stirred at the same temperature for 2 hours and then room temperature for 4 hours, 1M aqueous NaOH (1 mL) was added. After dilution with water and filtration with Celite, the insoluble material was washed with CHCl3. The aqueous phase was extracted with CHCl3 and combined organic layer was concentrated in vacuo. The residue was purified with silica-gel column chromatography to give 6-bromo-4-methylene-4H-spiro[chromene-3,3′-oxetane] (0.10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242973B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-89ae7d8a59da4d7bb4dc08eaba4b9aa1 |
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| Source note | uspto-grants-2016_01 |
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