Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930364Generated: October 31, 2026

Bicarbonate Ion → HCID 90373167, compound

https://huagongshe.com/reaction/930364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicarbonate IonHCID 769—
ReactantWaterHCID 962—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
ReactantHCID 86732184HCID 86732184—
SolventEthyl AcetateHCID 8857—
ProductHCID 90373167HCID 90373167—

Reaction Steps

Titan (IV)-ethoxide tech. (0.298 mL, 1.441 mmol) was added to a solution of (R)-2-methyl-2-propanesulfinamide (1.44 mmol) and 1-(5-bromo-2-fluoropyridin-3-yl)-2-fluoroethanone (170 mg, 0.720 mmol) in methylene chlorice (15 mL). The reaction mixture was stirred at room temperature (light-yellow solution) for 4 h (or until complete conversion by LCMS). The reaction mixture was poured into water and saturated aqueous bicarbonate solution and EtOAc were added. The suspension was stirred vigorously for 20 min. The organic phase was separated. The aqueous phase was extracted twice with EtOAc. The organic phases were combined and filtered through a pad of celite. The filtrate was washed with brine and dried over MgSO4. The solvent was removed under reduced pressure. The residue (239 mg of a yellow oil) was purified by column chromatography (silica gel, 10-70% hexanes/EtOAc) to yield (R,E)-N-(1-(5-bromo-2-fluoropyridin-3-yl)-2-fluoroethylidene)-2-methylpropane-2-sulfinamide as a yellow oil (106 mg; 43%). MS m/z=338.9 [M+H]+. Calculated for C11H13BrFN2OS: 339.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-d3c208eff2464ddbb71dec5f74c6b5ee
Source noteuspto-grants-2016_03