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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474638Generated: October 31, 2026

Tetrahydrofuran → HCID 66825615, compound

https://huagongshe.com/reaction/474638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantBenzonitrile, 2-[4-chloro-3-(trifluoromethyl)phenoxy]-5-formyl-HCID 86666201—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
ProductHCID 66825615HCID 6682561536.2%

Reaction Steps

To a solution of NaH (0.798 g, 19.96 mmol) in dry THF (15 mL) was added methyltriphenylphosphonium bromide (7.13 g, 19.96 mmol). The mixture was stirred at room temperature for 0.5 h. Then 2-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}-5-formylbenzonitrile (5.0 g, 15.35 mmol) was added. Stirring continued for 1.5 h, and the mixture was quenched by ice water. THF was removed by evaporation; the aqueous layer was extracted with DCM. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated to afford the title compound (1.8 g, 5.56 mmol, 36.2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-db6c85402d914284a45506163442fd60
Source noteuspto-grants-2014_01