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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356557Generated: November 2, 2026

Tetrahydrofuran → HCID 12072836, compound

https://huagongshe.com/reaction/1356557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 12072835HCID 12072835—
SolventWaterHCID 962—
ProductHCID 12072836HCID 1207283648.5%

Reaction Steps

A 1M tetrahydrofuran solution (7.0 ml) of a borane-tetrahydrofuran complex (7.0 mmol) was added dropwise to a tetrahydrofuran (20 ml) solution of (1R,2R,6S)-1-t-butoxycarbonylamino-4-p-anisoyl-4-azatricyclo[6.1.0.02,6]nonane (970 ml, 2.60 mmol) while cooling with ice, and the mixture was stirred at room temperature for 1 hour. While cooling with ice, water was added to the reaction mixture to decompose the excess borane-tetrahydrofuran complex. A 1N sodium hydroxide aqueous solution (10 ml) was added thereto, followed by refluxing for 6 hours. After cooling to room temperature, the reaction mixture was extracted with diethyl ether. The extract was dried over anhydrous sodium sulfate, the solvent was evaporated, and the residue was purified by silica gel column chromatography (chloroform:methanol=20:1) to give 453 mg (1.26 mmol, 48%) of the title compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586604B2
Source datasetuspto-grants-2003_07
ORD IDord-6824cd6418dc43edb7d07c8910070c08
Source noteuspto-grants-2003_07