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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454709Generated: October 31, 2026

Trifluoroacetic acid → HCID 58508568, compound

https://huagongshe.com/reaction/454709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantThioanisoleHCID 7520—
ReactantHCID 66991010HCID 66991010—
ProductHCID 58508568HCID 5850856877.8%

Reaction Steps

Thioanisole (2.0 mL) and trifluoroacetic acid (6.8 mL) were added to the obtained tert-butyl 2-(2-(benzyloxy)-5-(morpholin-4-yl)benzamido)-4-(thiophen-2-yl)benzoate (0.19 g), followed by stirring at room temperature for 24 hours. The solvent was evaporated under reduced pressure, and ethyl acetate was added to the residue. The solid substance was collected by filtration, and water and 2-propanol were added to the obtained solid substance. After adjusting the pH to 6.0 with a saturated aqueous solution of sodium bicarbonate, the solid substance was collected by filtration to obtain 0.11 g of 2-(2-hydroxy-5-(morpholin-4-yl)benzamido)-4-(thiophen-2-yl)benzoic acid as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-04eb784c68194421818a87ac3513974a
Source noteuspto-grants-2013_07