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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782112Generated: November 3, 2026

Dicyclohexylcarbodiimide → HCID 11976036, compound

https://huagongshe.com/reaction/1782112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-HydroxythiobenzamideHCID 2759344—
ReactantHCID 66738398HCID 66738398—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 11976036HCID 1197603648%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 4- or 5-tert-butoxycarbonylamino-2-hydroxy-benzoic acid (2) (3.0 mmol) in 50 mL of dimethylformamide, hydroxybenzotriazole (3.3 mmol) and DCC (3.3 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture, 4-hydroxy-thiobenzamide (3.0 mmol) was added and stirred mechanically for 3 h at 0°C. and 72 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure to remove the solvent. The oily residue thus obtained was dissolved in ethyl acetate; the organic layer washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude intermediate (7) was treated with a solution of 40% TFA in CH2Cl2. After 2 h the solvent was removed to obtain compound (8) as a crude residue. The residue was loaded on a silica gel open column and eluted with CH2Cl21MeOH (8/2), from which 4- or 5-Amino-2-hydroxy-benzoic acid 4-thiocarbamoyl-phenyl ester (8), compound of Formula XXVII, was obtained (48% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498355B2
Source datasetuspto-grants-2009_03
ORD IDord-91f794e2c45f4da0aa5f8a5161f797bb
Source noteuspto-grants-2009_03