HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichlorobenzaldehyde → HCID 86610813, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichlorobenzaldehyde | HCID 13404 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 86610812 | HCID 86610812 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86610813 | HCID 86610813 | — |
Reaction Steps
To a solution of 4-methyl-2-oxo-2H-chromene-6-carbonitrile (56 mg, 0.325 mmol) in dry THF (12 mL) at −20° C. was added drop wise 1.0 M LiHMDS solution in THF (0.6 mL). After 30 minutes 2,4-dichlorobenzaldehyde (105 mg) was added into the reaction mixture and the reaction mixture was stirred for 1 hour. The reaction mixture was then quenched with saturated aqueous ammonium chloride (10 mL) and extracted with ethyl acetate (50 mL). The organic layer was separated and dried over sodium sulfate, then concentrated and purified on silica gel eluted with 30%-60% ethyl acetate in hexanes to yield 4-[2-(2,4-dichloro-phenyl)-2-hydroxy-ethyl]-2-oxo-2H-chromene-6-carbonitrile as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662975B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-44b65971521f42d9bfbba7a8310c730f |
| Source note | uspto-grants-2010_02 |