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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081214Generated: November 3, 2026

Hydrochloric Acid → HCID 54304054, compound

https://huagongshe.com/reaction/1081214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButyl nitriteHCID 10996—
ReactantDecaneHCID 15600—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54304054HCID 54304054—

Reaction Conditions

Temperature5 °C

Reaction Steps

A cooled (-20° C.) solution of 8-ketotricyclo[5.2.1.0]decane (7.51 g, 50 mmol) in anhydrous tetrahydrofuran (50 mL) under nitrogen was treated with n-butyl nitrite (6.70 mL, 5.92 g, 57.3 mmol), then with solid potassium t-butoxide (11.22 g, 100 mmol) in portions at a rate to keep the pot temperature below -10° C. The red mixture was stirred at -10° C. for one h. and at 5° C. for 3.5 h, then it was quenched by addition to ice water (125 mL). The mixture was treated with concentrated hydrochloric acid (11 mL, 132 mmol), then the aqueous solution was extracted with methylene chloride (150 mL, then 2×100 mL). The combined organic solution was washed with saturated aqueous sodium bicarbonate (2×100 mL), water (100 mL), dried (Na2SO4), and concentrated in vacuo. The residue was chromatographed on silica gel (eluted with 5% acetone/methylene chloride) to afford tricyclo[5.2.1.0 (2,6)]decan-8,9-dione, oxime (4.88 g, 54.5%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583221
Source datasetuspto-grants-1996_12
ORD IDord-4b2d87d5ff004368ad90c30813df375b
Source noteuspto-grants-1996_12