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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170835Generated: October 30, 2026

Phosgene → HCID 90411618, compound

https://huagongshe.com/reaction/2170835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 2812134HCID 2812134—
SolventDichloromethaneHCID 6344—
ProductHCID 90411618HCID 9041161833%

Reaction Steps

N′-(4-fluorophenyl)thiophene-2-carbohydrazide (575 mg, 2.43 mmol) was dissolved in dichloromethane (14 mL) and tetrahydrofuran (10 mL) in a glass flask. The flask was cooled in ice. Phosgene (20% in toluene, 3.42 mL, 6.49 mmol, 2.67 eq.) was added, and the solution was stirred overnight under a nitrogen atmosphere, allowing it to warm to room temperature. Ethyl acetate (40 mL) was added, and the solution was then washed with water (2×25 mL) and brine (25 mL). The solution was dried over magnesium sulfate, filtered and concentrated in vacuo to give 0.59 grams of crude product as a light brown solid. Purification using ISCO flash chromatography (silica, gradient heptanes/ethyl acetate) gave 3-(4-fluorophenyl)-5-(thiophen-2-yl)-1,3,4-oxadiazol-2(3H)-one (210 mg, 0.800 mmol, yield 33.0%) as an off-white solid with an HPLC purity of 99.7%. LC-MS [M+H] 263.02 (C12H7FN2O2S+H, expected 263.02). The 1H-NMR spectrum was in accordance with the chemical structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051309B2
Source datasetuspto-grants-2015_06
ORD IDord-796b49372129477abc2202f19c07733c
Source noteuspto-grants-2015_06