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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196817Generated: November 2, 2026

Water → HCID 53940263, compound

https://huagongshe.com/reaction/1196817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 6-bromohexanoateHCID 117544—
ProductHCID 53940263HCID 5394026362%

Reaction Steps

223.12 g (1 mol) of ethyl 6-bromohexanoate and 275.4 g (1.05 mol) of triphenyl phosphine were refluxed for 36 hours in 1.5 l of acetonitrile. After the reaction was terminated, 500 ml of acetonitrile was distilled off, then the reaction mixture was dried. Into the dried mixture, 72.11 g (1 mol) of isobutyl aldehyde was added and stirred. Controlling the reaction temperature in the range of 25°-35° C., 40 g (1 mol) of oily (60%) sodium hydride was carefully added. Then, the reaction mixture was stirred over night at room temperature. After the reaction was ended, 500 g of water was added into the reaction mixture, the oil layer was then separated and the water layer was extracted twice with 300 ml of hexane. The organic layers were combined and washed with 300 ml of water, solvent was removed in vacuum under reduced pressure, and then distilled under 2 mm Hg to obtain 122.8 g of ethyl 8-methyl-6-nonenoate (Yield: 62% based upon the starting material).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116813
Source datasetuspto-grants-1992_05
ORD IDord-5b4fc81ab9d04fb48250514c911a55cb
Source noteuspto-grants-1992_05