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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019185Generated: November 1, 2026

4-Bromothioanisole → 2-Trimethylsilyloxy-4'-(methylthio)isobutyrophenone

https://huagongshe.com/reaction/1019185

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromothioanisoleHCID 66037—
ReactantMethyl 2-methyl-2-[(trimethylsilyl)oxy]propanoateHCID 14297555—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-Trimethylsilyloxy-4'-(methylthio)isobutyrophenoneHCID 1840019033.6%

Reaction Conditions

Temperature-78 °C

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 2.5 M 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. 1H NMR (CD3COCD3) d 0.05 (9H, s), 1.52 (6H, s), 2.53 (3H, s), 7.33 (2H, d), 8.12 (2H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486194B2
Source datasetuspto-grants-2002_11
ORD IDord-2f1474bc66c648238c2a3db68ca10966
Source noteuspto-grants-2002_11