HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654761Generated: November 2, 2026
Benzaldehyde → 1-Phenyl-3-(trimethylsilyl)-2-propyn-1-ol
https://huagongshe.com/reaction/1654761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Phenyl-3-(trimethylsilyl)-2-propyn-1-ol | HCID 2760416 | 100.1% |
Reaction Steps
Place lithium hexamethyldisilazane (20 mL of a 1M solution in tetrahydrofuran, 20 mmol) under an argon atmosphere and cool to 0° C. Add, by dropwise addition, trimethylsilylacetylene (2.83 mL, 20 mmol) and stir for 1 hour at 0° C. Add benzaldehyde (2.03 mL, 20 mmol) in tetrahydrofuran (10 mL). Allow to warm to room temperature and stir for 1 hour. Pour the mixture into ethyl ether and water, separate the organic phase and evaporate the solvent in vacuo. Filter the oil through silica gel (20% ethyl acetate/hexane) and evaporate the solvent in vacuo to yield 4.09 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05409942 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-499b7b88eb184209b78aee6d29f2b4f9 |
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| Source note | uspto-grants-1995_04 |
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