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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18917Generated: October 28, 2026

Methanol → HCID 57934778, compound

https://huagongshe.com/reaction/18917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 2-amino-5-tert-butylthiophene-3-carboxylateHCID 15541821—
SolventWaterHCID 962—
ProductHCID 57934778HCID 5793477896%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a vial containing methyl 5-tert-butyl-2-aminothiophene-3-carboxylate (0.643 g) in 1:1 methanol: H2O (6 mL) was added KOH (0.5069 g). The vial was capped and the mixture was stirred at 80° C. for 6 h. The solvent was removed under vacuum and the crude product was dissolved in water (50 mL) and transferred to a 100 mL round bottom flask. To the vigorously stirred aqueous solution was added at room temperature drop wise phosgene (2M toluene, 6 mL) over a 15 minute period. The resulting mixture was stirred at room temperature overnight. The crude reaction mixture was filtered; the precipitate was washed with water, dried and dissolved in ethyl acetate (10 mL). The organic solution was dried over anhydrous sodium sulfate, filtered and the solvent was removed under vacuum to give 654.9 mg (96%) of the expected 6-tert-butyl-1H-thieno[2,3-d][1,3]oxazine-2,4-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741479B2
Source datasetuspto-grants-2010_06
ORD IDord-23bb3b7255a2406cb1eb3f414505a56f
Source noteuspto-grants-2010_06