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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245745Generated: November 1, 2026

Naphthalene → HCID 59216880, compound

https://huagongshe.com/reaction/2245745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNaphthaleneHCID 931—
ReactantTriethylamineHCID 8471—
ReactantTrichlorosilaneHCID 24811—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59216873HCID 59216873—
SolventDiethyl EtherHCID 3283—
SolventO-XyleneHCID 7237—
ProductHCID 59216880HCID 5921688089.3%

Reaction Conditions

Temperature4 °C

Reaction Steps

(−)-5-(Diphenylphosphinoyl)-6-(2-methoxynaphthalen-1-yl)-4,7-dimethyl-1,3-dihydroisobenzofuran (800 mg, 1.59 mmol, 92% ee) was placed into a flask and the atmosphere in the flask was replaced with nitrogen. Triethylamine (4.4 mL, 31.8 mmol) was added to a solution of this naphthalene compound in xylene (40 mL), and cooled to 4° C. Further, trichlorosilane (800 μL, 7.95 mmol) was added dropwise, and the mixture was stirred for 30 minutes and then stirred at room temperature for 15 minutes. Further, the reaction mixture was heated to 110° C. and stirred for 3 hours. After the resulting reaction mixture was cooled to room temperature, diethyl ether (60 mL) and saturated aq. sodium bicarbonate (800 μL) were added, and the mixture was stirred for 30 minutes. The reaction mixture was filtered through Celite, and after the filtrate was dried with sodium sulfate. After silica gel was added, the mixture was concentrated under reduced pressure. The residue was purified by silica gel chromatography to obtain the title compound (694 mg, 89%, 92% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683186B2
Source datasetuspto-grants-2010_03
ORD IDord-abbcf75f03754d40aebd3c4a6a367f2b
Source noteuspto-grants-2010_03