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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360033Generated: October 30, 2026

Diethyl cyanophosphonate → HCID 57419479, compound

https://huagongshe.com/reaction/2360033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant5-Bromo-1-indanoneHCID 520695—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57419479HCID 57419479—

Reaction Steps

To a solution of 5-bromo-2,3-dihydro-1H-inden-1-one (1 g, 4.74 mmol) in anhydrous THF (15 ml) at −10° C. was added 2M lithium diisopropylamide in THF (0.242 ml, 0.483 mmol) dropwise. The resulting mixture was stirred at −10° C. for 15 min before diethylcyanophosphonate (0.791 ml, 5.21 mmol) was added dropwise. Following the addition, the mixture was allowed to warm to room temperature, and was stirred at room temperature for 3 h. The mixture was cooled to −78° C. and borontrifluoride diethyl etherate (1.196 ml, 9.52 mmol) was added dropwise. Following the addition, the mixture was stirred at −78° C. for 1 h and was then allowed to warm to room temperature and was stirred at room temperature for 16 h. The mixture was concentrated in vacuo, and the residue was partitioned between EtOAc (50 mL) and H2O (2×50 mL). The organic layer was dried over Na2SO4, filtered and concentrated in vacuo, and the crude product was purified by column chromatography on silica gel using 9:1 EtOAc:hexanes as the eluent. The title compound was obtained as an tan solid (0.72 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685991B2
Source datasetuspto-grants-2014_04
ORD IDord-999b90a09c44417cb3ddcd2de325b990
Source noteuspto-grants-2014_04