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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335912Generated: October 30, 2026

Boron tribromide → HCID 58466135, compound

https://huagongshe.com/reaction/335912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 59272305HCID 59272305—
SolventDichloromethaneHCID 6344—
ProductHCID 58466135HCID 58466135—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2′-bromo-1′-fluoro-7′-methoxy-5H-spiro[oxazole-4,9′-xanthen]-2-amine (0.575 g, 1.516 mmol) in 15 mL of CH2Cl2 at −15° C. was added boron tribromide (1.0 M in CH2Cl2, 4.55 mL, 4.55 mmol). The mixture was slowly allowed to warm to 0° C. over the course of 1.25 hours at which point the reaction was carefully quenched with 2 mL of MeOH and saturated sodium bicarbonate (100 mL). This mixture was poured into a separatory funnel containing EtOAc (100 mL). The layers were separated and the aqueous layer was extracted with EtOAc (2×100 mL). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to provide 2-amino-2′-bromo-1′-fluoro-5H-spiro[oxazole-4,9′-xanthen]-7′-ol as a glassy red solid. MS m/z=365.1 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-1cb1d0bdfeb8429f849515853cb48c3b
Source noteuspto-grants-2014_11