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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434634Generated: November 1, 2026

tert-Butanol → HCID 15411266, compound

https://huagongshe.com/reaction/1434634

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantEthyl AcetateHCID 8857—
ReactantSodiumHCID 5360545—
ReactantHCID 14936170HCID 14936170—
CatalystMercuryHCID 23931—
SolventHCID 18619786HCID 18619786—
ProductHCID 15411266HCID 1541126645%

Reaction Steps

A 2.5% Na amalgam was prepared by adding sodium (15.1 g, 657 mmol) slices to mercury (56 mL, 3.77 mol). This amalgam was added in portions to a vigorously stirring solution of NaH2PO4 (24.4 g, 203 mmol) and Na2HPO4 (28.9 g, 203 mmol) in a 1:1 tert-butanol:ethyl acetate mixture (100 mL). A solution of 7-tert-Butoxycarbonyl-2-p-tolylsulfonyl-7-azabicyclo[2.2.1]-hepta-2-ene (14.22 g, 40.7 mmol) in a 1:1 tert-butanol-ethyl acetate mixture (200 mL) was added to the stirring mixture at 0° C. After stirring for 24 h the mixture was decanted into a separatory funnel and extracted with ethyl acetate. The remaining mercury was washed thoroughly 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 provide 7-tert-Butoxycarbonyl-7-azabicyclo[2.2.1]hept-2-ene (3-56 g, 45% based on recovered starting material) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615567B2
Source datasetuspto-grants-2009_11
ORD IDord-9b983d53856b43ae85f78d403f7406c7
Source noteuspto-grants-2009_11