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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174924Generated: November 2, 2026

Tetrahydrofuran → 2-Ethylsulfanyl-5-nitrobenzooxazole

https://huagongshe.com/reaction/1174924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant5-Nitrobenzo[D]Oxazole-2-ThiolHCID 786293—
CatalystIodoethaneHCID 6340—
Product2-Ethylsulfanyl-5-nitrobenzooxazoleHCID 5742149541%

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838543B2
Source datasetuspto-grants-2010_11
ORD IDord-2f6b9c423ecb4fee85f91e6a9c405226
Source noteuspto-grants-2010_11