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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437884Generated: November 2, 2026

Trifluoroacetic acid → HCID 57941426, compound

https://huagongshe.com/reaction/1437884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57941346HCID 57941346—
SolventDichloromethaneHCID 6344—
ProductHCID 57941426HCID 5794142672%

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoroacetic acid (15 mL) was added to a cooled (0° C.) solution of crude N′-(4-methoxy-phenyl)-N′-((1R,4R)-4,7,7-trimethyl-3-oxo-bicyclo[2.2.1]heptane-2-carbonyl)-hydrazinecarboxylic acid tert-butyl ester (˜18.5 mmol) in dichloromethane (15 mL), and the solution was stirred at ˜0° C. for 15 min and then at room temperature for 2.5 h. The solvent was evaporated and the residue was dissolved in dichloromethane (150 mL) and washed with water (4×250 mL) until the pH of the aqueous washing was ˜5. The organic layer was washed with brine (150 mL), dried (magnesium sulfate), and then the flask was wrapped in aluminum and stored in a freezer overnight. The magnesium sulfate was filtered off, and the solvent was evaporated to give an orange/red semi-solid which was triturated with 10% dichloromethane/hexanes, filtered, and washed with hexanes. The solid was crushed, washed again with hexanes, and then dried under vacuum to give (4S,7R)-2-(4-methoxy-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (3.95 g, 72%) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-a711c22e1a3042478da33f3759dfcd90
Source noteuspto-grants-2009_11