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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354819Generated: November 1, 2026

4-Fluorosalicylic acid → HCID 58865711, compound

https://huagongshe.com/reaction/1354819

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorosalicylic acidHCID 67661—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant(4-Amino-3-benzyloxyphenyl)-carbamic acid 9H-fluoren-9-ylmethyl esterHCID 58865047—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58865711HCID 5886571135%

Reaction Steps

4-Fluoro-2-hydroxy-benzoic acid (74) (0.15 g, 0.961 mmol) was dissolved in DMF (6 mL), 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl-uronium hexafluorophosphate (HBTU) (0.382 g, 1.01 mmol) was added followed by iPr2EtN (0.167 mL, 0.961 mmol) and the mixture was shaken in a Teflon septum capped 40 mL I-Chem vial at room temperature for 25 minutes. (4-Amino-3-benzyloxy-phenyl)-carbamic acid 9H-fluoren-9-ylmethyl ester (0.419 g, 0.961 mmol) was added and the mixture was shaken at room temperature for 16 h. LC-MS indicated complete coupling at this point. The mixture was diluted with EtOAc (50 mL), washed with water (25 mL), aqueous saturated NaHCO3 (25 mL) and brine (25 mL) via extraction, dried over MgSO4. The organic layer was concentrated to give a yellow oil. Purification by flash chromatography using a gradient of hexane and EtOAc (eluding with 15–100% EtOAc in hexane in 30 minutes) gave the desired product (75) upon concentration (0.192 g, 0.334 mmol, 35% yield). LC-MS (ESI): (exact mass: 574.19) m/e=575.2 [M+1]+ (100%), 1149.5 [2M+1]+ (25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223759B2
Source datasetuspto-grants-2007_05
ORD IDord-6f2a5964c9754fab84713bc594ecc608
Source noteuspto-grants-2007_05