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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975Generated: October 25, 2026

Hydrochloric Acid → tetraethyl N-benzyl-5-aminopentane-1,1-bisphosphonate

https://huagongshe.com/reaction/1975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactanttetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonateHCID 19689031—
SolventTetrahydrofuranHCID 8028—
Producttetraethyl N-benzyl-5-aminopentane-1,1-bisphosphonateHCID 1968905845.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of tetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonate (0.63 g, 1.36 mmol) in THF (3.4 mL) was cooled to 0° C., and borane methylsulfide (0.34 ml, 3.4 mmol) was added via syringe. The reaction was stirred at 0° C. for 20 minutes, then warmed to 65° C. for 2.5 hours. The reaction mixture was cooled to 0° C. and 6N HCl (4.0 ml) was added carefully. The solvent was removed in vacuo, and the residue was concentrated repeatedly from methanol (2×5 mL). The residue was dissolved in water (10 ml) and extracted with diethyl ether (3×5 ml). The aqueous layer was made basic to phenolphthalein with solid KOH and saturated with NaCl. The product was extracted into dichloromethane (5×20 ml), dried (Na2SO4) and concentrated to give the title compound (0.28 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728650
Source datasetuspto-grants-1998_03
ORD IDord-861d1c5c6eb14e7f813a68ed25b21881
Source noteuspto-grants-1998_03