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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544298Generated: November 2, 2026

Tetrahydrofuran → HCID 13092017, compound

https://huagongshe.com/reaction/544298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 13091979HCID 13091979—
ProductHCID 13092017HCID 13092017—

Reaction Steps

Ethyl 1-(2-chloro-6-fluorophenyl)-1-hydroxymethanecarboximidate hydrochloride (15.0 g., 0.056 mole) and triethylamine (16.8 g., 23.3 ml., 0.167 mole) were taken into 560 ml. of tetrahydrofuran and cooled to 0° C. Phosgene was bubbled through the reaction mixture for 35 minutes. It was then stirred for 2.5 hours at room temperature, poured into 600 cc. of crushed ice and extracted with three portions of ethyl acetate. The combined extracts were washed with water, washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to product (14.4 g.). Recrystallization from toluene afforded purified 5-(2-chloro-6-fluorophenyl)oxazolidine-2,4-dione [10.7 g., 83%; m.p. 153°-155° C.; ir (KBr) 1820, 1740 cm-1 ].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448971
Source datasetuspto-grants-1984_05
ORD IDord-e8cfcbf4c1c84508afeed4123f16f722
Source noteuspto-grants-1984_05