HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185244Generated: October 30, 2026
Toluene → 6-Bromo-4,4-dimethyl-2-methylene chroman
https://huagongshe.com/reaction/2185244
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2H-1-Benzopyran-2-one, 6-bromo-3,4-dihydro-4,4-dimethyl- | HCID 22568923 | — |
| Catalyst | mu-Chlorobis(eta5-cyclopentadienyl)(dimethylaluminum)-mu-methylenetitanium | HCID 53384502 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 6-Bromo-4,4-dimethyl-2-methylene chroman | HCID 18710222 | 74% |
Reaction Steps
A stirred, cooled (ice bath) solution of 6-bromo-4,4-dimethyl-chroman-2-one available in accordance with U.S. Pat. No. 5,399,561 incorporated herein by reference (1 g, 3.92 mmol) in 8 mL of anhydrous tetrahydrofuiran was treated with a 0.5 M solution of μ-chloro-μ-methylene-[ bis(cyclopentadienyl)titanium]dimethylaluminum (Tebbe reagent) in toluene (8.23 mL, 4.12 mmol). After 10 minutes, the reaction mixture was poured into ice-water mixture containing 50 mL of 1M sodium hydroxide and extracted with hexane. The hexane extract was washed with brine (×1), filtered over a bed of celite and evaporated in vacuo to an oil which was subjected to flash column chromatography over silica gel (230-400 mesh) using hexane as the eluent to afford the title compound (0.74 g, 74%) as a clear oil. 1H NMR (300 MHz, CDCl3): δ 7.34 (d, 1H, J=2.3 Hz), 7.23 (dd, 1H, J=2.3, 8.5 Hz), 6.77 (d, 1H, J=8.0 Hz), 4.61 (d, 1H, J=0.73 Hz), 4.17 (d, 1H, J=0.73 Hz), 2.33 (s, 2H), 1.27 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399774B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-f5436c976a424a42a8ab5d19617228ae |
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| Source note | uspto-grants-2002_06 |
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