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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27792Generated: October 26, 2026

Methyl vinyl ketone → 5-Nonyn-2-one, 9-chloro-

https://huagongshe.com/reaction/27792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl vinyl ketoneHCID 6570—
ReactantBoron trifluoride etherateHCID 8000—
Reactant1-Pentyne, 5-chloro-HCID 84308—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
Product5-Nonyn-2-one, 9-chloro-HCID 11435214—

Reaction Steps

14.85 Parts of 5-chloropent-1-yne is dissolved in 250 parts by volume of toluene and the resulting solution is cooled to approximately -40°. To that solution is then added 62.8 parts by volume of 2.31 M ethereal butyl lithium and stirring is continued for approximately 15 minutes. 6.87 Parts of boron trifluoride etherate is added and the reaction mixture is stirred for about 2 hours, then allowed to stand for about 16 hours at -5° to -10°. At the end of that time 10.14 parts of methyl vinyl ketone is added at -40° and the reaction mixture is stirred for about 4 hours, then is quenched with water. 50 Parts by volume of 3 N hydrochloric acid is added and the mixture is kept at room temperature for about 16 hours, at the end of which time the aqueous and organic layers are separated. The aqueous layer is extracted with toluene and the organic layer with water. The organic solutions are combined, washed successively with aqueous sodium hydroxide and water, then dried over anhydrous sodium sulfate and stripped to dryness under reduced pressure, thus affording the crude product. This material is purified by distillation under reduced pressure to afford 9-chloro-5-nonyn-2-one, boiling at about 80°-92° at a pressure of 0.11-0.06 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04223158
Source datasetuspto-grants-1980_09
ORD IDord-a6ca3969df8a4cf88b27b5f2f6b8a062
Source noteuspto-grants-1980_09