HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-Ethylsulfanyl-5-nitrobenzooxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Nitrobenzo[D]Oxazole-2-Thiol | HCID 786293 | — |
| Catalyst | Iodoethane | HCID 6340 | — |
| Product | 2-Ethylsulfanyl-5-nitrobenzooxazole | HCID 57421495 | 41% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Dissolve 5-Nitro-3H-benzooxazole-2-thione (10.58 g, 53.9 mmol) in anhydrous THF (300 mL). Cool the mixture to 0° C. in an ice bath. Add NaH (4.90 g, 60% dispersion in mineral oil) slowly. Stir the resulting mixture at 0° C. for 10 min. Add iodoethane (20.0 mL, 0.250 mmol) to the stirring mixture. Allow the mixture to warm to room temperature and stir overnight. Adsorb the reaction mixture onto silica gel and subject to flash column chromatography in 2 batches (330 g, 120 g columns, eluting with 10-50% ethyl acetate/n-hexane both times) to yield the desired product (4.93 g, 41%). 1H NMR (400 MHz, DMSO-d6): δ 8.47 (d, J=2.4 Hz, 1H), 8.23 (dd, J=9.2, 2.6 Hz, 1H), 7.88 (d, J=8.8 Hz, 1H), 3.37 (q, J=6.8 Hz, 2H), 1.45 (t, J=7.6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902356B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-47ff2f3263c041feb1cb74c47e9c7ecb |
| Source note | uspto-grants-2011_03 |