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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690778Generated: October 31, 2026

Sodium Sulfite → 3-[5-(Tetrahydro-pyran-4-yl)-1,3-dihydro-isoindole-2-carbonyl]-4-((s)-2,2,2-trifluoro-1-methyl-ethoxy)-benzenesulfinate sodium salt

https://huagongshe.com/reaction/1690778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 56851160HCID 56851160—
SolventWaterHCID 962—
Product3-[5-(Tetrahydro-pyran-4-yl)-1,3-dihydro-isoindole-2-carbonyl]-4-((s)-2,2,2-trifluoro-1-methyl-ethoxy)-benzenesulfinate sodium saltHCID 5685116148%

Reaction Conditions

Temperature37.5 °C

Reaction Steps

1.15 g (8.94 mmol) of Na2SO3 and 1.70 g (9.60 mmol) of Na2HPO4 hydrate were dissolved in 13 ml water. An ethanolic solution of 2.40 g (4.63 mmol) of 3-[5-(tetrahydro-pyran-4-yl)-1,3-dihydro-isoindole-2-carbonyl]-4-((S)-2,2,2-trifluoro-1-methyl-ethoxy)-benzenesulfonyl chloride was added. The reaction mixture was stirred at 35 to 40° C. during 1 hour and then overnight at room temperature. 1.3 g Speedex was added, the reaction mixture was filtered and the filtrate was evaporated. The crude product was treated with aqueous citric acid/NaCl solution then extracted with MTBE/THF 1:1. The organic solvent was evaporated and the residue was dissolved in MeOH/water (2:1), and treated with 800 mg (9.52 mmol) of NaHCO3. 1 g Speedex was added and the reaction mixture was filtrated and concentrated in vacuo. The residue was purified chromatographically by using a reverse phase column (RP-18, water/methanol) to provide 1.12 g (48%) of the title compound as a white foam. MS (m/e): 484.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153679B2
Source datasetuspto-grants-2012_04
ORD IDord-770876c0155c4979912b5baf0b37c5dc
Source noteuspto-grants-2012_04