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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938191Generated: October 31, 2026

Thioxanthone → 9-cyclopropyl-9H-thioxanthen-9-ol

https://huagongshe.com/reaction/1938191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioxanthoneHCID 10295—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418630HCID 178418630—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product9-cyclopropyl-9H-thioxanthen-9-olHCID 18799335—

Reaction Steps

A solution of cyclopropylmagnesium bromide in dry THF (prepared from cyclopropylbromide (18.2 g, 0.15 mol), magnesium turnings (2.9 g, 0.12 mol) and dry THF (80 ml)) was placed under an atmosphere of nitrogen. A solution of thioxanthen-9-one (12.7 g, 0.06 mol) in dry THF (70 ml) was added dropwise and when addition was complete the mixture was heated at reflux for 20 minutes. The reaction mixture was cooled on an ice-bath and saturated ammonium chloride (70 ml) was carefully added. The mixture was diluted with water (100 ml) and extracted with diethyl ether (2×100 ml). The combined organic extracts were washed with water, dried (Na2SO4) and the solvent was evaporated in vacuo to give 25.2 g of crude 9-cyclopropyl-9H-thioxanthen-9-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693649
Source datasetuspto-grants-1997_12
ORD IDord-add6b1bc3ab74ca1858c3fa91ec0c8fa
Source noteuspto-grants-1997_12