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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494089Generated: October 29, 2026

Ammonia → 5-Carbomethoxy-oct-7-enenitrile

https://huagongshe.com/reaction/1494089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 10081040HCID 10081040—
ReactantHCID 14986661HCID 14986661—
ReactantMethyl 5-methoxycarbonyl-oct-7-enoateHCID 14986662—
SolventMethanolHCID 887—
Product5-Carbomethoxy-oct-7-enenitrileHCID 14986703—

Reaction Steps

Methyl 1-allyl-2-oxocyclopentane-1-carboxylate (1.1 Kg) is added to 1,100 mL of methanol previously saturated with ammonia gas at ice bath temperature. The reaction mixture is stirred first at ice bath temperature and then at room temperature overnight with constant introduction of ammonia. The reaction mixture is evaporated to dryness to yield starting material and a mixture of 5-carbomethoxyoct-7-enoic acid amide and methyl 5-carbomethoxy-oct-7enoate. The residue is distilled under reduced pressure to yield a mixture of the diester and ester amide. A portion (25 g) is added dropwise over 40 minutes to 23.6 g of thionyl chloride and the mixture is heated at 80° for 30 minutes. The reaction mixture is evaporated to dryness under water vacuum and then distilled under high vacuum to yield 5-carbomethoxy-oct-7-enenitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025025
Source datasetuspto-grants-1991_06
ORD IDord-04d4bf0d781844c98d76519c4eba0fca
Source noteuspto-grants-1991_06