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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650713Generated: November 1, 2026

Tetrafluoroborate → HCID 21713174, compound

https://huagongshe.com/reaction/650713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroborateHCID 26255—
ReactantHCID 21713168HCID 21713168—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
ProductHCID 21713174HCID 21713174102.5%

Reaction Steps

(E)-2-Propyl-3-phenylsulfonylacrylic acid (0.3 g, 1.18 mmol) was dissolved in degassed methanol (15 ml) and [(S,S)-EtDuPHOS Rh (COD)]BF4 (8 mg, 1.18×10−2 mmol) was added under a stream of nitrogen. This solution was injected into the pressure vessel under nitrogen, and then the bomb was charged with hydrogen. The mixture was hydrogenated at 2070 kPa (300 psi) for 3 hour at room temperature. The methanol was removed under reduced pressure to give the title compound (0.31 g, 100% yield). E.e. was determined by chiral HPLC to be 92% e.e. [Chiropak AD; 5% ethanol-95% heptane; 1 ml/min; 254 nm; major enantiomer Rf 18.46 min., minor enantiomer Rf 15.22 min.]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274758B1
Source datasetuspto-grants-2001_08
ORD IDord-c6316d96986a4f16a0594c5dc77950a7
Source noteuspto-grants-2001_08