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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281390Generated: October 31, 2026

Potassium Carbonate → 8-(Benzoxazol-2-ylsulfanyl)octylamine

https://huagongshe.com/reaction/1281390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-(8-Bromooctyl)phthalimideHCID 253681—
Reactant1,3-benzoxazole-2-thiolHCID 178418282—
SolventDimethylformamideHCID 6228—
Product8-(Benzoxazol-2-ylsulfanyl)octylamineHCID 22237518—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a round bottom flask with 2-mercaptobenzoxazole (2.14 g, 14.2 mmol) and DMF (100 mL) at room temperature was added K2CO3 (2.61 g, 18.9 mmol) followed by N-(8-bromooctyl)phthalimide (4.00 g, 11.8 mmol). The resulting solution was heated to 60° C. for 0.5 h and then cooled back to room temperature. At this point, the reaction mixture was quenched with H2O (100 mL) and then diluted with EtOAc (600 mL). The organic layer was washed with 1 N HCl (60 mL), sat. aq. NaHCO3 (60 mL), and brine (60 mL) and then dried (MgSO4). After concentration, the residue was purified by the Biotage Flash 40 apparatus (10 to 20% EtOAc/petroleum ether gradient) to afford the thioether intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451827B2
Source datasetuspto-grants-2002_09
ORD IDord-827df001ff2344139f5580614e523315
Source noteuspto-grants-2002_09