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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193947Generated: November 1, 2026

Benzyl Bromide → HCID 22496209, compound

https://huagongshe.com/reaction/2193947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 22496346HCID 22496346—
SolventDimethylacetamideHCID 31374—
ProductHCID 22496209HCID 2249620966.3%

Reaction Steps

A solution of 6-phenyl-1H-thieno[3,2-d][1,3]oxazine-2,4-dione (1 g, 4.1 mmol) and anhydrous sodium carbonate (477 mg, 4.5 mmol) diluted in 15 ml of anhydrous dimethylacetamide was stirred for one hour under nitrogen before adding benzyl bromide (785 mg, 4.5 mmol). The mixture was stirred overnight at room temperature. 912 mg (66.3%) of 1-benzyl-6-phenyl-1H-thieno[3,2-d][1,3]oxazine-2,4-dione were obtained as a pale yellow solid after filtration and washing the precipitate with acetone and pentane. NMR 1H (DMSO D6, 400 MHz): 7.8-7.76 ppm (m, 3H, Haro); 7.51-7.45 ppm (m, 3H, Haro); 7.43-7.41 ppm (m, 2H, Haro); 7.35-7.3 ppm (m, 2H, Haro); 7.28-7.24 ppm (m, 1H, Haro); 5.22 ppm (s, 1H, NCH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329924B2
Source datasetuspto-grants-2012_12
ORD IDord-b701ae9b95a94d2d92f360d97273619f
Source noteuspto-grants-2012_12