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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003783Generated: October 30, 2026

4-Aminobenzylphosphonic acid → 1,8-Diazabicyclo(5.4.0)undec-7-ene

https://huagongshe.com/reaction/1003783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzylphosphonic acidHCID 223978—
SolventTetrahydrofuranHCID 8028—
Product1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184983.4%
Product4-Aminobenzylphosphonic acidHCID 223978—

Reaction Steps

A round-bottom reaction flask (25 ml) equipped with a magnetic stirrer was fitted with a septum and a cool-trap condenser. It was charged with C60 (NO2) (100 mg) and tetrahydrofuran (15 ml). The solution was added 4-aminobenzylphosphonic acid (150 mg) in tetrahydrofuran (5 ml) and treated under sonication conditions for 30 min at ambient temperatures. At the end of reaction, suspended solids in the solution were separated by a centrifuge technique and repeatedly washed with tetrahydrofuran and acetone. The resulting brown solids were dried in vacuum at 40° C. to afford the corresponding 4-aminobenzylphosphonic acid derivatives of C60, C60 [--NHC6H4CH2P(=O) (OH)3 ]n, (95 mg) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 400 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046361
Source datasetuspto-grants-2000_04
ORD IDord-df7fd4317f6a41b992ddcfee29528e2b
Source noteuspto-grants-2000_04