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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912470Generated: October 26, 2026

Diethyl Ether → HCID 67417764, compound

https://huagongshe.com/reaction/912470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(6-bromo-5-(2,4-difluorophenoxy)-1H-indazol-1-yl)-2-methylpropan-2-olHCID 67416478—
ReactantHCID 86631053HCID 86631053—
SolventDichloromethaneHCID 6344—
ProductHCID 67417764HCID 6741776478%

Reaction Steps

A solution of 1-(6-Bromo-5-(2,4-difluorophenoxy)-1H-indazol-1-yl)-2-methylpropan-2-ol (19.8 g, 49.8 mmol) in DCM (150 mL) was cooled with a dry-ice acetone bath to −73° C. (Diaminoethyl)sulfur trifluoride (6.9 mL, 52.3 mmol) was added dropwise over 2 min; the temperature rose to −62° C. The resulting solution was stirred in the bath for a further 1 hr, then at ambient temperature for 1 hour. The reaction mixture was poured into a separatory funnel containing cold 10% KOH (250 mL), and then diethyl ether (500 mL) was added. After shaking, the organic layer was washed with brine (150 mL), dried over sodium sulfate and evaporated. The residue was chromatographed on silica gel using 85/15 hexanes/EtOAc as eluent. Fractions containing product were pooled and the solvent removed under reduced pressure to afford the title compound as an orange oil (13.4 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026233B2
Source datasetuspto-grants-2011_09
ORD IDord-a43a133e445343b4a29d62e794ed0f52
Source noteuspto-grants-2011_09