HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989817Generated: November 2, 2026
2-(3-Bromo-4-methoxyphenyl)-2-methylpropanal → 2-Bromo-4-(1,1-dimethyl-allyl)-1-methoxy-benzene
https://huagongshe.com/reaction/1989817
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(3-Bromo-4-methoxyphenyl)-2-methylpropanal | HCID 11161190 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-4-(1,1-dimethyl-allyl)-1-methoxy-benzene | HCID 11242261 | — |
Reaction Steps
A suspension of methyltriphenylphosphonium bromide (7.71 g, 0.0215 mol) in dry THF (100 mL) was cooled to 0° C. under argon. n-BuLi (2.5M, 8 mL, 0.020 mol) was added slowly. The resulting clear orange solution of the ylide was stirred for another 15 min at 0° C. 2-(3-Bromo-4-methoxy-phenyl)-2-methyl-propionaldehyde (3.7 g, 0.014 mol) was dissolved in dry THF (50 mL) and added to ylide-solution. The mixture was stirred for 3 h/25° C. and the resulting suspension was quenched with MeOH (10 mL). The solvent was removed under reduced pressure and the crude product was purified by flash chromatography using n-heptane as eluent. Yield: 3.1 g (84%). GCMS: >99%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642367B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-8aa25e99d5f64f8f8502362ecd780eb6 |
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| Source note | uspto-grants-2010_01 |
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