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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601546Generated: October 29, 2026

Tetrahydrofuran → 2-Ethylsulfanyl-5-nitrobenzooxazole

https://huagongshe.com/reaction/601546

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 numberUS07902356B2
Source datasetuspto-grants-2011_03
ORD IDord-47ff2f3263c041feb1cb74c47e9c7ecb
Source noteuspto-grants-2011_03