HuagongsheHuagongshe Chemistry Print Report · For research reference only
Xanthene → HCID 86662011, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Xanthene | HCID 7107 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86662011 | HCID 86662011 | 36.7% |
Reaction Steps
Referring to Scheme 5, bromoacetyl chloride (4.59 ml, 54.9 mmol) was added dropwise to a solution of 9H-xanthene (5 g, 27.4 mmol) and AlCl3 (8.05 g, 60.4 mmol), DCM (100 mL) at 0° C. The reaction mixture was allowed to warm up to rt and left to stir for 72 h. The reaction mixture was poured onto ice (400 mL), extracted with DCM (2×200 mL). The combined organic phase was washed with brine (400 mL), dried over MgSO4, filtered and evaporated to dryness. The crude material was precipitated in EtOAc and filtered to give 1,1′-(9H-xanthene-2,7-diyl)bis(2-bromoethanone) (5-2) as a white solid (4.27 g, 36.7% yield). LC-MS (ESI): m/z 425.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150554B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-8a8c72ef2a094f91ae33321c91cc77cc |
| Source note | uspto-grants-2015_10 |