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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260588Generated: November 1, 2026

Trimethylsilylacetylene → 1-methoxy-4-(trimethylsilyl)-3-Butyn-2-one

https://huagongshe.com/reaction/1260588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantN,2-dimethoxy-N-methylacetamideHCID 14872187—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-methoxy-4-(trimethylsilyl)-3-Butyn-2-oneHCID 8586002179.7%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of 14.75 ml of trimethylsilylacetylene (103.62 mmol) in 250 ml of tetrahydrofuran is cooled to −70° C. and then 64.76 ml of a 1.6 M solution of n-BuLi (103.62 mmol) in hexane are added. The mixture is stirred for 25 minutes at −70° C. and then a solution of 13.14 g of N-methoxy-N-methyl-2-methoxyacetamide (98.69 mmol) in 250 ml of tetrahydrofuran is added rapidly. During the addition, the temperature rises to −50° C., and then the cold bath is removed and the mixture is stirred for 2 hours at ambient temperature. A 1N solution of HClaq is added and then extraction is carried out 4 times with ethyl acetate. The organic phases are combined, dried over sodium sulphate, filtered, and concentrated under vacuum. 13.4 g of 1-methoxy-4-(trimethylsilyl)but-3-yn-2-one are obtained in the form of a light brown oil which is used without subsequent purification (crude yield=80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470847B2
Source datasetuspto-grants-2013_06
ORD IDord-63adfd495ef6440585648bfab1fc55e3
Source noteuspto-grants-2013_06