HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324073Generated: October 29, 2026
Potassium Carbonate → 8-(Benzoxazol-2-ylsulfanyl)octylamine
https://huagongshe.com/reaction/324073
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(8-Bromooctyl)phthalimide | HCID 253681 | — |
| Reactant | 1,3-benzoxazole-2-thiol | HCID 178418282 | — |
| Product | 8-(Benzoxazol-2-ylsulfanyl)octylamine | HCID 22237518 | — |
Reaction Steps
To a round bottom flask with 2-mercaptobenzoxazole (2.14 g, 14.2 mmol) andDMF (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06214877B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-e138183fe99946a18669d49ad5bab428 |
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| Source note | uspto-grants-2001_04 |
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