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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885379Generated: October 25, 2026

4-Bromothioanisole → Dimethyl 2-thioanisylterepthalate

https://huagongshe.com/reaction/1885379

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromothioanisoleHCID 66037—
ReactantDimethyl 2-bromoterephthalateHCID 87741—
ReactantHCID 178418306HCID 178418306—
CatalystBis(triphenylphosphine)nickel(II)chlorideHCID 84306—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl 2-thioanisylterepthalateHCID 86744855—

Reaction Steps

4-Bromothioanisole (7.1 g) was dissolved in tetrahydrofuran (23 ml). To this solution at -78° C. under nitrogen was added over a ten minute period 1.7M tBuLi (48 ml). After 45 minutes at room temperature, 1M ZnCl2 (41 ml) was added dropwise over a ten minute period. After one half hour at room temperature, bis(triphenylphosphine)nickel (II) chloride (1.4 g) was added followed by dimethyl-2-bromoterepthalate (4.67 g) in tetrahydrofuran (47 ml). The reaction mixture was stirred at room temperature for 45 minutes. The THF was removed under reduced pressure. The residue was treated with ethyl acetate and 1N HCl and the layers separated. The organic phase was washed with water, brine, dried over magnesium sulfate and evaporated gave the crude product. Chromatography on silica gel using 15% ethyl acetate/hexanes gave the desired product (3.92 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05144028
Source datasetuspto-grants-1992_09
ORD IDord-7b007aac96c4449dbda050f0741bda68
Source noteuspto-grants-1992_09