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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659509Generated: November 2, 2026

Ammonia → 6-Octenoic acid, 7-methyl-3-oxo-, ethyl ester

https://huagongshe.com/reaction/1659509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthyl AcetoacetateHCID 8868—
Reactant1-Chloro-3-methyl-2-buteneHCID 10429—
ReactantSodiumHCID 5360545—
CatalystSodiumHCID 5360545—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product6-Octenoic acid, 7-methyl-3-oxo-, ethyl esterHCID 1051216538.4%

Reaction Steps

A mixture of 1.4 g of ferric nitrate in 1200 ml of liquid ammonia was formed at -60° C. and was then stirred for 5 minutes after which 2 g of sodium were added thereto at -60° C. The mixture was stirred for 10 minutes and 104 g of sodium were added at -55±5° C. over 21/2 hours. The mixture was stirred at -55° C. for one hour. 300 g of ethyl acetylacetate were added thereto over 30 minutes at less than -30° C. 1000 ml of ether at -20° C. were added to the mixture which was then stirred for 5 minutes. 289 g of 1-chloro-3-methyl-2-butene were added over 30 minutes at less than -25° C. and the mixture stood at room temperature for 17 hours. 1000 ml of ether were progressively added at less than ±15° C. followed by a solution of 250 ml of acetic acid in 1000 ml of water. The decanted aqueous phase was extracted with ether and the combined organic phases were washed with 2 N hydrochloric acid, then with water, dried over sodium sulfate and evaporated to dryness under reduced pressure. The residue was rectified under reduced pressure to obtain 175.5 g of ethyl 7-methyl-3-oxo-6-octenoate with a boiling point of 98° to 107° C. at 3 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04304733
Source datasetuspto-grants-1981_12
ORD IDord-e096e2d576dd4cdcabb62b9bfd36969a
Source noteuspto-grants-1981_12