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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862475Generated: November 3, 2026

Hydrochloric Acid → HCID 14936170, compound

https://huagongshe.com/reaction/1862475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 2-(4-methylbenzene-1-sulfonyl)-7-azabicyclo[2.2.1]hepta-2,5-diene-7-carboxylateHCID 14936167—
CatalystNickel acetate tetrahydrateHCID 62601—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14936170HCID 1493617073%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of nickel (II) acetate tetrahydrate (161 g, 647 mmol) in ethanol (400 mL) was added dropwise a solution of sodium borohydride (24.6 g, 1.54 mol) in ethanol (500 mL). This mixture was cooled to 0° C. and a solution of 7-tert-Butoxycarbonyl-2-p-tolylsulfonyl-7-azabicyclo[2.2.1]-hepta-2,5-diene (44.49 g, 128 mmol) in THF (300 mL) was added. Concentrated HCl (100 mL) was next added and the mixture allowed to stir overnight. After quenching the reaction with sodium bicarbonate, the mixture was filtered over a celite pad and extracted several times with ethyl acetate. The combined organic layers were dried with sodium sulfate, concentrated, then purified by flash chromatography with 4:1 hexane:ethyl acetate to give 7-tert-Butoxycarbonyl-2-p-tolylsulfonyl-7-azabicyclo[2.2.1]-hepta-2-ene (32.57 g, 73%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538010B1
Source datasetuspto-grants-2003_03
ORD IDord-e8aaf8bb2557405d80c5668f5b8ab247
Source noteuspto-grants-2003_03