HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161040Generated: October 29, 2026
Potassium Carbonate → 3-[{4-[(4-Acetyl-3-hydroxy-2-methyl-phenylamino)-methyl]-phenyl}-(tetrahydro-pyran-2-yloxy)-methyl]-benzonitrile
https://huagongshe.com/reaction/1161040
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 57438306 | HCID 57438306 | — |
| Reactant | 1-(4-Amino-2-hydroxy-3-methyl-phenyl)-ethanone | HCID 57438308 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[{4-[(4-Acetyl-3-hydroxy-2-methyl-phenylamino)-methyl]-phenyl}-(tetrahydro-pyran-2-yloxy)-methyl]-benzonitrile | HCID 66699550 | 64% |
Reaction Steps
To a solution of 1-(4-amino-2-hydroxy-3-methyl-phenyl)-ethanone (300 mg, 1.8 mmol) and 3-[(4-Iodomethyl-phenyl)-(tetrahydro-pyran-2-yloxy)-methyl]-benzonitrile (865 mg, 2.0 mmol)) in anhydrous DMF (1.5 mL) under Ar gas at RT is added K2CO3 (303 mg, 2.2 mmol). The reaction mixture is heated at 50° C. overnight. The reaction mixture is quenched into water and extracted with EtOAc (3×). The organic layers are combined, washed with brine, dried over Na2SO4 and concentrated. The residue is purified by flash chromatography using 25% EtOAc/hexane as eluent. Obtained is the title compound as a yellow foam (538 mg, 64%). LC-MS (m/e): 469 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816523B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-9cccf387e8c2404685b9f4facb86c73e |
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| Source note | uspto-grants-2010_10 |
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