HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromophenol → 8-Bromo-2H-1-benzopyran-3(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 8-Bromo-2H-1-benzopyran-3(4H)-one | HCID 19087148 | — |
Reaction Steps
8-Bromochroman-3-one 28B was prepared from 2-bromophenol in a manner similar to that described in the literature (J. Med. Chem., 1988, 689): Reaction of 2-bromophenol with paraformadehyde (MgCl2, NEt3, THF, 75° C., 4 h), followed by treatment with acrylonitrile (neat, Dabco, 95° C., 18 h), and hydrolysis with 10% NaOH (100° C., 4 h) afforded 28A. Compound 28A was reacted with DPPA (NEt3, toluene, 110° C., 2 h) followed by treatment with 6N HCl (85° C., 2 h) to afford 8-bromochroman-3-one 28B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476274B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-a7b38cbe1a26428e8ae99f36e4d59cb7 |
| Source note | uspto-grants-2013_07 |