HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370873Generated: October 30, 2026
Allyl m-bromophenyl ether → HCID 18512295, compound
https://huagongshe.com/reaction/1370873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl m-bromophenyl ether | HCID 257945 | — |
| Reactant | HCID 18511970 | HCID 18511970 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18512295 | HCID 18512295 | 36% |
Reaction Steps
The product from Example 88C (0.983 g, 3.80 mmoles) in anhydrous THF (10 mL) at −78° C. was treated dropwise with 1.7 M t-butyllithium (4.46 mL, 7.59 mmoles). Reaction stirred 30 minutes at −78° C. and was then treated with the product from Example 88B (1.00 g, 1.90 mmoles. Reaction stirred 15 minutes at −78° C. and then allowed to warm to 0° C. Reaction quenched with saturated NH4Cl and warmed to room temperature. The mixture was diluted with ethyl acetate, washed with H2O, brine, dried (Na2SO4), filtered, and the filtrate concentrated under reduced pressure. The residue was purified by chromatography on a pre-packed Biotage silica gel column (30% ethyl acetate:hexanes) to provide the title compound (0.369 g, 36%). MS (ESI−) m/z 539 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06583180B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-a6db85bf35c34c1aa1abf9671abf24c2 |
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| Source note | uspto-grants-2003_06 |
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