Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455625Generated: October 31, 2026

Potassium Hydroxide → (S)-(9-amino-2-bromo-7-iodo-9H-xanthen-9-yl)methanol

https://huagongshe.com/reaction/455625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant(S)-2'-bromo-7'-iodospiro[oxazolidine-4,9'-xanthen]-2-oneHCID 67383335—
SolventDioxane MethanolHCID 21966525—
Product(S)-(9-amino-2-bromo-7-iodo-9H-xanthen-9-yl)methanolHCID 6738344637%

Reaction Steps

In a 350-mL resealable vessel, the (S)-2′-bromo-7′-iodospiro[oxazolidine-4,9′-xanthen]-2-one (11 g, 24.02 mmol) was dissolved in 1:1 MeOH-dioxane (160 mL). Aqueous KOH (5 M, 48.0 mL, 240 mmol) was added. The vessel was sealed and placed in a 105° C. oil bath. After 24 h, the reaction was concentrated to remove the MeOH and most of the dioxane. The residue was diluted with water (200 mL) and the aqueous phase was extracted with 5% MeOH-DCM (4×200 mL). The organics were combined, washed with dilute brine (35 mL), dried over sodium sulfate and concentrated. The residue was purified by chromatography (1.5% MeOH/DCM) to afford (S)-(9-amino-2-bromo-7-iodo-9H-xanthen-9-yl)methanol (3.84 g, 8.89 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497264B2
Source datasetuspto-grants-2013_07
ORD IDord-afd4f1f069454a5f90b8cd2920ca173d
Source noteuspto-grants-2013_07