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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940164Generated: October 30, 2026

4-Bromothioanisole → HCID 18788503, compound

https://huagongshe.com/reaction/1940164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromothioanisoleHCID 66037—
ReactantCornforth reagentHCID 2724130—
Reactant2-Cyclopenten-1-one, 2-bromo-HCID 3014641—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18788503HCID 18788503—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a -78° C. solution of 4-bromothioanisole (35.1 g, 173 mmol) in THF (500 mL) was added nBuLi (1.6M in hexanes, 107.5 mL, 172 mmol). The solution was stirred for 45 min, then a solution of 2-bromo-2-cyclopenten-1-one (25.4 g, 158 mmol) in THF (150 mL) was added and the mixture was allowed to warm to 0° C. and was quenched with saturated aqueous NH4Cl. The majority of the solvent was removed in vacuo and the residue was suspended in water and extracted with two portions of EtOAc. The organic layers were washed with brine, dried over MgSO4, faltered and concentrated. This material was dissolved in DMF (300 mL), cooled to 0° C. and treated with PDC (72.4 g, 192 mmol). The resulting mixture was warmed to r.t. and stirred for 2 h, then poured into H2O (1.2 L) and extracted with two 500 mL portions of EtOAc. The organic layers were washed with brine, dried over MgSO4, filtered and concentrated to give the title compound as a light brown solid which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05698584
Source datasetuspto-grants-1997_12
ORD IDord-dac6f6b265164b8596140bba166a8853
Source noteuspto-grants-1997_12