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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747005Generated: October 29, 2026

Xanthene → HCID 86662011, compound

https://huagongshe.com/reaction/1747005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantXantheneHCID 7107—
ReactantBromoacetyl chlorideHCID 89602—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 86662011HCID 8666201136.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150554B2
Source datasetuspto-grants-2015_10
ORD IDord-8a8c72ef2a094f91ae33321c91cc77cc
Source noteuspto-grants-2015_10