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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302045Generated: October 31, 2026

6-Hydroxyquinoline → HCID 13663813, compound

https://huagongshe.com/reaction/2302045

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-HydroxyquinolineHCID 11374—
ReactantTriphenylphosphineHCID 11776—
ReactantTricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13663813HCID 1366381319.6%

Reaction Steps

A mixture of 1-adamantanemethanol (5.00 g, 30.0 mmol) and 6-hydroxyquinoline (13.1 g, 90.2 mmol) in tetrahydrofuran (75 mL) was stirred for 15 min. Then, triphenylphosphine (10.2 g, 39.0 mmol) was added, followed by diethyl azodicarboxylate (6.14 mL, 39.0 mmol). The reaction mixture was refluxed for 18 h. The solvent was then removed by rotary evaporation. The resulting gel was filtered through paper with diethyl ether (3×25 mL). The filtrate was rotary evaporated, and the resulting gel was filtered through paper with hexanes (3×25 mL). Again the filtrate was rotary evaporated, the resulting gel was filtered through paper with hexanes (3×25 mL), and the filtrate was rotary evaporated. This provided 3.8 g (43%) of crude product as a red oil. This oil was chromatographed (2:1 hexanes/ethyl acetate) to provide 1.6 g (18%) of (94):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06429207B1
Source datasetuspto-grants-2002_08
ORD IDord-cc8923e990b74c6e8d2ed1591e4d2ab7
Source noteuspto-grants-2002_08