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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972982Generated: November 1, 2026

6-Bromo-2-(methylsulfanyl)-1,3-benzothiazole → HCID 58529564, compound

https://huagongshe.com/reaction/1972982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2-(methylsulfanyl)-1,3-benzothiazoleHCID 17953514—
ReactantHCID 178419772HCID 178419772—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductHCID 58529564HCID 5852956428%

Reaction Conditions

Temperature60 °C

Reaction Steps

A degassed mixture of 6-bromo-2-(methylthio)-1,3-benzothiazole (4.20 g, 16.14 mmol), tetrakis(triphenylphosphine)palladium(0) (186 mg, 0.161 mmol) and benzylzinc bromide (0.5 M in THF, 61.34 mL) was heated at 60° C. for 4 hrs. EtOAc (200 mL) was added and the organic layer was washed with saturated, aqueous NaHCO3 (3×150 mL), then water (3×150 mL). The organic layer was dried over MgSO4 and concentrated. The crude material was purified by ISCO® chromatography using 4% EtOAc in hexane to obtain the desired product (1.50 g, 28%). 1H NMR (400 MHz, acetone-d6) δ 8.20 (s, 1H), 7.88 (d, 1H), 7.62 (d, 1H), 7.44-7.30 (m, 5H), 4.44 (s, 2H); LC-MS m/z [M+H]+ 304.2 & 306.1, RT 4.02 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-4fa96f02d4174bdfab06bae037068e36
Source noteuspto-grants-2013_04