HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (S)-(9-amino-2-bromo-7-iodo-9H-xanthen-9-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (S)-2'-bromo-7'-iodospiro[oxazolidine-4,9'-xanthen]-2-one | HCID 67383335 | — |
| Solvent | Dioxane Methanol | HCID 21966525 | — |
| Product | (S)-(9-amino-2-bromo-7-iodo-9H-xanthen-9-yl)methanol | HCID 67383446 | 37% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497264B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-afd4f1f069454a5f90b8cd2920ca173d |
| Source note | uspto-grants-2013_07 |