HuagongsheHuagongshe Chemistry Print Report · For research reference only
Xanthydrol → ethyl 2-(4-bromo-2-methylbenzoyl)-2-(9H-xanthen-9-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Xanthydrol | HCID 72861 | — |
| Reactant | Ethyl 3-(4-bromo-2-methylphenyl)-3-oxopropanoate | HCID 53404613 | — |
| Solvent | Acetic acid ethanol | HCID 18476134 | — |
| Product | ethyl 2-(4-bromo-2-methylbenzoyl)-2-(9H-xanthen-9-yl)acetate | HCID 53697250 | — |
Reaction Steps
A solution of ethyl 2-methyl-4-bromobenzoylacetate (18.5 g, 65.0 mmol) was heated at 60° C. with 9-hydroxyxanthene (14.2 g, 71.5 mmol) in ethanol-acetic acid (1:1, 200 ml) for 40 h. The product was isolated as in Example 1 (iii), except the aqueous phase was extracted with diethyl ether. The crude product was purified on flash silica eluting with hexane-dichloromethane (3:2 then 1:1) to give ethyl 2-(4-bromo-2-methylbenzoyl)-2-(9H-xanthen-9-yl)acetate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891899 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-b115eb2db3a3424eb10f50ab7694ef6f |
| Source note | uspto-grants-1999_04 |