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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454682Generated: October 30, 2026

Chloroform → HCID 58508891, compound

https://huagongshe.com/reaction/454682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantHCID 66990348HCID 66990348—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 58508891HCID 5850889185.3%

Reaction Steps

To a solution mixture of the obtained tert-butyl 2-(2-(benzyloxy)-5-(piperidin-1-yl)benzamido)-4-phenoxybenzoate (0.093 g) in ethyl acetate (1.5 mL) and methanol (1.5 mL), 10% palladium-carbon (0.047 g) was added, followed by stirring under a hydrogen atmosphere at room temperature for 2 hours. Chloroform was added to the reaction mixture. The insoluble substance was removed by filtration, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Kanto Chemical Co., Inc., silica gel 60 (spherical), eluent: 80-70% hexane/ethyl acetate] to obtain 0.067 g of tert-butyl 2-(2-hydroxy-5-(piperidin-1-yl)benzamido)-4-phenoxybenzoate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-43d58093b9e745efb2d4db9be0060b48
Source noteuspto-grants-2013_07