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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388419Generated: November 1, 2026

Bromine → HCID 58432991, compound

https://huagongshe.com/reaction/388419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1,1-Dimethylethyl 3-(4-chlorophenyl)-4-isothiazolecarboxylateHCID 58432986—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58432991HCID 58432991—

Reaction Steps

A solution of 8 (3.50 g) in THF (60 ml) is cooled to −78° C. under N2 followed by drop wise addition of BuLi (8.0 ml, 1.6M in hexane). After complete addition stirring is continued at −78° C. for 15 min. Bromine (1.2 ml) is now added drop wise and stirring is continued at −78° C. for 15 min, after which the cooling bath is removed. The mixture is allowed to warm to room temp. TLC shows a good conversion into a slightly faster moving spot (Hep/EA, 9/1). 1N HCl (50 ml) is added and the THF is removed in vacuo. Water (100 ml), containing some sodium thiosulfate, is added and the product is extracted with EtOAc (150 ml). The organic layer is washed with sat. NaHCO3, brine, dried and concentrated. The orange/red oily residue is purified by flash column chromatography (˜50 g silica, 5% diisopropyl ether in heptane) yielding 3.1 g of 9 as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377953B2
Source datasetuspto-grants-2013_02
ORD IDord-a97795fa1fd740c3969ee2efc93f8305
Source noteuspto-grants-2013_02