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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055584Generated: November 4, 2026

Potassium Carbonate → 2-(2-Fluoro-6-methoxyphenyl)-1,2-thiazinane 1,1-dioxide

https://huagongshe.com/reaction/2055584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-ButanesultamHCID 303508—
Reactant2-Bromo-3-fluoroanisoleHCID 2779318—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
Product2-(2-Fluoro-6-methoxyphenyl)-1,2-thiazinane 1,1-dioxideHCID 69266206—

Reaction Steps

2-Bromo-1-fluoro-3-methoxybenzene (200 mg, 0.975 mmol), 1,2-thiazinane 1,1-dioxide (264 mg, 1.951 mmol), copper (62 mg, 0.975 mmol) and potassium carbonate (270 mg, 1.95 1 mmol) were combined and heated to 170 C for 5 hours. After this time, the mixture was suspended in methanol (15 ml) and vortexed for 18 hours. This mixture was filtered through Gelman Acrodisc and evaporated in vacuo. The resulting residue was partitioned between EtOAc (2×10 ml) and aq NH4Cl (5 ml). The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo. This residue was purified by column chromatography eluting with a 0-10% EtOAc/CH2Cl2 to give 2-(2-fluoro-6-methoxyphenyl)-1,2-thiazinane 1,1-dioxide. Low resolution mass spectrometry: (M+H+)=260.1. 1H NMR (400 MHz, CDCl3) δ 7.21 (dt, 1H, J=8.1 and 4.3 Hz), 6.69-6.77 (m, 21), 3.88 (s, 3H), 3.75-8.74 (m, 1H), 3.65 (dq, 1H, J=4.6, 6.0 and 14 Hz), 3.24 (dd, 2H, J=5.6 and 7.4 Hz), 3.27 (quin, 2H, J=6.1 Hz) and 1.78-1.90 (m, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332499B2
Source datasetuspto-grants-2008_02
ORD IDord-93c57c96160d4b989e601d9dd1fb5deb
Source noteuspto-grants-2008_02