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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17533Generated: October 28, 2026

Acetic Acid → HCID 68587091, compound

https://huagongshe.com/reaction/17533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
ReactantStannous chloride dihydrateHCID 61436—
ReactantHCID 68586542HCID 68586542—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 68587091HCID 6858709190%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-[(3S)-3-(Dimethylamino)pyrrolidin-1-yl]-4-nitrobiphenyl-3-carbonitrile (I-242) (7.9 g, 23.5 mmol) was dissolved in concentrated hydrochloric acid (40 ml), and at room temperature, acetic acid (4.0 ml, 70.5 mmol) and methanol (10 ml) were added, followed by cooling at 0° C., and tin(II) chloride dihydrate (15.9 g, 70.5 mmol) was gradually added. After stirred at the same temperature for 20 minutes, this was further stirred at room temperature for 20 minutes. At room temperature, methanol (30 ml) was added to the suspension, followed by stirring at the same temperature for 24 hours. The reaction liquid was fractionated with ethyl acetate and aqueous 1 M sodium hydroxide solution. The organic layer was washed with saturated brine, then dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was subjected to column chromatography with silica gel, and the fraction with chloroform:methanol=95:5 gave the entitled compound (6.475 g, 90%) as a pale brown gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737166B2
Source datasetuspto-grants-2010_06
ORD IDord-a40ef0f6b3394eb8975030275c29634e
Source noteuspto-grants-2010_06