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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175828Generated: November 1, 2026

Hydrochloric Acid → Bicyclo(2.2.2)octane-1,4-diamine dihydrochloride

https://huagongshe.com/reaction/1175828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantBicyclo[2.2.2]octane-1,4-dicarboxylic acidHCID 607709—
SolventTolueneHCID 1140—
ProductBicyclo(2.2.2)octane-1,4-diamine dihydrochlorideHCID 6842423987.4%

Reaction Steps

A suspension of 1,4-dicarboxybicyclo[2.2.2]octane (9.91 g, 50 mmol) in toluene (225 mL) was azeotroped under a Dean-Stark trap to dryness, then cooled to room temperature under nitrogen and treated with triethylamine (20 mL, 143 mmol) and diphenylphosphoryl azide (33.0 g, 120 mmol). The solution was slowly and cautiously warmed to 80° C. (some exotherm and much evolution of gas observed) and stirred at 80°-90° C. for 3 h, then concentrated in vacuo to remove toluene and the residue cooled on an ice bath and treated with 6N hydrochloric acid (150 mL, 900 mmol). The bath was removed and the mixture stirred at room temperature for 3 h, then partially concentrated to remove most water. Acetonitrile (600 mL) was added, and the suspension was cooled for an hour in a refrigerator, filtered, and the solid rinsed with acetonitrile and dried in vacuo to afford 9.31 g (87%) of subject material as a white solid. [M+H]+=141.3. 1H NMR (d6-DMSO) δ 8.24 (br s, 6H), 1.81 (s, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842707B2
Source datasetuspto-grants-2010_11
ORD IDord-c8701b809f684a2e8d0900d92dde9659
Source noteuspto-grants-2010_11