HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 6-bromo-3,3-bis(hydroxymethyl)-2,2-dimethyl-2,3-dihydro-4H-chromen-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 6-bromo-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one | HCID 14755364 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-bromo-3,3-bis(hydroxymethyl)-2,2-dimethyl-2,3-dihydro-4H-chromen-4-one | HCID 86724244 | 86.6% |
Reaction Steps
To a mixture of 6-bromo-2,2-dimethyl-2,3-dihydro-4H-chromen-4-one (1.00 g, 3.92 mmol) and dioxane (10 mL) were added formaldehyde (37 wt. % in water, 2.95 mL, 39.2 mmol) and Na2CO3 (831 mg, 7.84 mmol) at room temperature. After stirring overnight at the same temperature, the reaction mixture was filtered. The filtrate was diluted with CHCl3, washed with 1M aqueous HCl and water, dried over MgSO4 and filtered. The filtrate was concentrated at reduced pressure, and the residue was purified with column chromatography on silica gel (hexane-EtOAc, a linear gradient of EtOAc from 0 to 50%) to afford 6-bromo-3,3-bis(hydroxymethyl)-2,2-dimethyl-2,3-dihydro-4H-chromen-4-one (1.07 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242973B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-b10ef795afca4f99afe05562872d01ba |
| Source note | uspto-grants-2016_01 |