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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773117Generated: November 1, 2026

Ammonium Chloride → 9-Chloro-1,1-diethoxy-2-nonyne

https://huagongshe.com/reaction/1773117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl orthoformateHCID 31214—
Reactant1-Octyne, 8-chloro-HCID 90360—
ReactantHCID 178418332HCID 178418332—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product9-Chloro-1,1-diethoxy-2-nonyneHCID 1407471575.3%

Reaction Conditions

Temperature47.5 °C

Reaction Steps

In a reactor equipped with a stirrer, a cooling condenser, a dropping funnel and a thermometer was placed a solution of methyl magnesium chloride (89.7 g:1.2 mol) in tetrahydrofuran (370.0 g), and stirred at a solution temperature of from 45 to 50° C. The 8-chloro-1-octyne (144.6 g:1.0 mol) was dropwise added thereto at a reaction mixture temperature of from 50 to 60° C. over one hour, and then stirred at from 60 to 65° C. for 5 hours. A solution of triethyl orthoformate (177.8 g:1.2 mol) in toluene (120.0 g) was then dropwise added thereto at a reaction mixture of from 80 to 85° C. over 30 minutes, and stirred at from 90 to 95° C. for 6 hours. After completion of the reaction was confirmed by gas chromatography, acetic acid (57.0 g), ammonium chloride (35.0 g) and water (400.0 g) were added to the reaction mixture. The organic phase separated from the aqueous phase was washed with an aqueous 1.0% sodium hydroxide solution (170.0 g). The organic phase was subjected to removal of the solvent under reduced pressure, and then the residue was distilled under reduced pressure to obtain 9-chloro-1,1-diethoxy-2-nonyne [bp: 138-142° C./0.13 KPa, 185.8 g, 0.75 mol]. [Yield: 75.3%]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255056B2
Source datasetuspto-grants-2016_02
ORD IDord-495df89b77614d31a2b21b0b6cc80d81
Source noteuspto-grants-2016_02