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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626442Generated: October 30, 2026

Tetrahydrofuran → 5808-99-1

https://huagongshe.com/reaction/626442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
ReactantCyclopropanecarboxaldehydeHCID 123114—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5808-99-1HCID 53401852—

Reaction Steps

At 0° C., 13.0 ml (64.85 mmol) of ethyl diethylphosphonoacetate were added dropwise to a suspension of 2.59 g (64.85 mmol) of sodium hydride (60% in mineral oil) in 110 ml of abs. THF. After 30 min, the mixture was warmed to RT and, after cooling again to 0° C., 5.3 ml (71.34 mmol) of cyclopropanecarboxaldehyde were added dropwise. After the end of the addition, the reaction mixture was warmed to RT and diluted with 35 ml of DMF. The mixture was stirred at RT overnight and then added to water. The mixture was extracted three times with ethyl acetate. The combined organic phases were concentrated under reduced pressure and the crude product was purified by filtration through silica gel (mobile phase cyclohexane/ethyl acetate 10:1→6:1). This gave 8.53 g of the target product (93.8% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309198B2
Source datasetuspto-grants-2016_04
ORD IDord-629f24e922994f8a9e8f0bc6ae0776f1
Source noteuspto-grants-2016_04