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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477633Generated: November 1, 2026

Dichloromethane → HCID 117839182, compound

https://huagongshe.com/reaction/1477633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 117849117HCID 117849117—
SolventEthyl AcetateHCID 8857—
ProductHCID 117839182HCID 117839182—

Reaction Steps

To a dichloromethane solution (32 mL) of tert-butyl (S)-4-(4-fluorophenyl)-5-(pivaloyloxy)-5,6-dihydropyridine-1(2H)-carboxylate (1.62 g, 4.29 mmol) synthesized in Reference Synthesis Example 136, trifluoroacetic acid (6.5 mL) was added and the resultant mixture was stirred at room temperature for 20 hours. After completion of the reaction, saturated sodium bicarbonate aqueous solution was added to the reaction solution and extraction from the resultant mixture with ethyl acetate was performed. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain the title compound as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-b2e33c7d0ec64e7ea79556f40daac06f
Source noteuspto-grants-2016_08