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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | N,2-dimethoxy-N-methylacetamide | HCID 14872187 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-methoxy-4-(trimethylsilyl)-3-Butyn-2-one | HCID 85860021 | 79.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470847B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-63adfd495ef6440585648bfab1fc55e3 |
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| Source note | uspto-grants-2013_06 |
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