HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 7-Ethyl-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 7-Bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole | HCID 12148969 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Ethyl-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole | HCID 11482966 | 91% |
Reaction Steps
n-Butyllithium (2.5 N, 0.43 mL, 1.08 mmol) was added dropwise into a cold (−78° C.) mixture of 7-bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole (300 mg, 0.90 mmol) and THF (2 mL). The mixture was allowed to stir for 0.5 h. Iodoethane (0.14 mL, 1.8 mmol) was added dropwise into the mixture. The reaction mixture was allowed to warm to room temperature and stirred for 2 h. The reaction was quenched with aqueous ammonium chloride, poured into water, and extracted with EtOAc. The organic extracts were washed with brine and dried over MgSO4. Evaporation and flash chromatography (20% EtOAc/petroleum ether) gave (231 mg, 91% yield) of the product as a light brown solid: m.p. 85° C.; MS m/e 284 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531564B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-1346cc4e34af4b6584e9a4e01ce0ae14 |
| Source note | uspto-grants-2009_05 |