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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206955Generated: October 31, 2026

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

https://huagongshe.com/reaction/2206955

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 numberUS09376368B2
Source datasetuspto-grants-2016_06
ORD IDord-170af14d71bb419bb96ade5b781dbc83
Source noteuspto-grants-2016_06