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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607804Generated: October 26, 2026

Sulfuric Acid → 16-(m-Methylphenoxy)hexadeca-5,8,11,14-tetraynoic acid methyl ester

https://huagongshe.com/reaction/1607804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantMethyl 7-iodohept-5-ynoateHCID 10901527—
Reactant9-(m-Methylphenoxy)-1,4,7-nonatriyneHCID 14578973—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product16-(m-Methylphenoxy)hexadeca-5,8,11,14-tetraynoic acid methyl esterHCID 14578974—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.61 ml (751 mg, 5.6 mmol) of 3.6N ethylmagnesium bromide in ether was added dropwise, under argon to a solution of 1.34 g (6 mmol) of 9-(m-methylphenoxy)-1,4,7-nonatriyne in 20 ml of anhydrous tetrahydrofuran. The temperature was maintained at 0° C. The reaction mixture was stirred for one hour further at 0° C., then allowed to warm to room temperature, and then 50 mg of cuprous cyanide wasadded. The mixture was stirred for 20 minutes, heated to 40° C. and then 1 g (3.75 mmol) of 7-iodo-5-heptynoic acid methyl ester was added. The resulting mixture was stirred during 4 hours at 40° C. The reaction mixture was then poured into 60 ml of 1N sulfuric acid and ice and the product extracted with ether (3×100 ml). The combined organic extract was concentrated to about 1/5 its original volume and washed several times with EDTA and water, dried over sodium sulfate and evaporated in vacuo. The crude material was purified by column chromatography on 75 g of silica gel, using hexane:ethyl acetate (85:15) as eluant, to obtain 16-(m-methylphenoxy)hexadeca-5,8,11,14-tetraynoic acid methyl ester, as an oil. The product was stored in dry ice.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04867915
Source datasetuspto-grants-1989_09
ORD IDord-a02baf2b8ebc4dba88a78f697c7979e4
Source noteuspto-grants-1989_09