HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735451Generated: October 30, 2026
4-Bromothioanisole → 2-Trimethylsilyloxy-4'-(methylthio)isobutyrophenone
https://huagongshe.com/reaction/1735451
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromothioanisole | HCID 66037 | — |
| Reactant | Methyl 2-methyl-2-[(trimethylsilyl)oxy]propanoate | HCID 14297555 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Trimethylsilyloxy-4'-(methylthio)isobutyrophenone | HCID 18400190 | 33.6% |
Reaction Steps
A solution of 204 mg (1.0 mmol) of 4-bromothioanisole in 2.5 mL of THF was cooled to -78° C. and treated with 0.42 mL of 2.5M n-BuLi solution in hexane. After stirring at -78° C. for 1 h, a solution of 380 mg (2.0 mmol) of methyl 2-trimethylsilyloxyisobutyrate in 2 mL of THF was added. The mixture was stirred at -78° C. for 2 h and then quenched with NH4OAc buffer. The product was extracted with EtOAc, dried over MgSO4 and concentrated. The residue was purified by flash chromatography, eluting with 19:1 hexane/EtOAc to give 95 mg of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05536752 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-e7e27248db214cd5aad0450a9fba8c32 |
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| Source note | uspto-grants-1996_07 |
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